SR-4(3): Validate as Genuine and Not Altered
SR-4(3): Validate as Genuine and Not Altered requires you to verify, at receipt, that each system or system component is authentic and has not been tampered with before you deploy it into your environment. Operationalize it by defining acceptance checks, assigning an owner, recording results for every receipt event, and enforcing quarantine and escalation when checks fail.
Key takeaways:
- Treat “receipt validation” as a gate in procurement and receiving, not a one-time policy statement.
- Build a standard checklist: provenance, packaging integrity, cryptographic/signature checks (where available), and chain-of-custody documentation.
- Evidence matters as much as execution; auditors will ask for per-receipt records and exception handling.
The sr-4(3): validate as genuine and not altered requirement sits in the Supply Chain Risk Management (SR) control family in NIST SP 800-53 Rev. 5 and focuses on a simple operational outcome: don’t install or connect components you cannot trust. For a Compliance Officer, CCO, or GRC lead, the practical challenge is less about understanding the intent and more about converting it into a repeatable receiving process that procurement, IT operations, and asset management will actually follow.
This control is easiest to pass (and easiest to fail) at the seams: third-party purchasing, drop-shipments, urgent replacement parts, and remote site deliveries. If you cannot show a consistent “acceptance gate” with records, you will struggle to demonstrate that your organization reliably prevents counterfeit, substituted, or modified components from entering production.
This page gives requirement-level implementation guidance you can put into a control procedure quickly: who owns what, what to check, what artifacts to retain, and what exam teams typically challenge. It also includes a pragmatic execution plan and FAQs for the edge cases that break many programs.
Regulatory text
NIST SR-4(3) text (excerpt): “Employ the following controls to validate that the system or system component received is genuine and has not been altered: {{ insert: param, sr-4.3_prm_1 }}.” 1
Operator interpretation: NIST is directing you to put concrete receipt-validation controls in place. The placeholder parameter indicates the organization must define the specific validation methods it will employ (for example, packaging inspection, serial number verification, cryptographic validation, approved distribution channels), document them, and perform them consistently for each receipt event before the component is introduced into the system environment. 2
Plain-English interpretation (what the requirement means)
You must be able to answer, with evidence: “For this device/software/component we received, how did we verify it was authentic and unchanged from what we ordered, and what did we do when it didn’t pass?”
This is not limited to “hardware in a box.” Scope typically includes:
- End-user devices, servers, network gear, and IoT/OT components.
- Replaceable parts (drives, NICs, PSUs) and spares.
- Software media, firmware updates, appliances, and pre-built images.
- Cloud “components” when they are delivered as images/appliances you import into your tenant (for example, marketplace appliances), where you have an intake step.
Who it applies to (entity and operational context)
Entity types: Federal information systems and contractor systems handling federal data commonly implement NIST SP 800-53 controls, including SR-4(3). 2
Operational contexts that must be in scope:
- Procurement and third-party sourcing: Where the item is ordered and who it is ordered from.
- Receiving and inventory intake: Where the item is accepted, tagged, and recorded.
- IT/OT operations: Where the item is staged, configured, and deployed.
- Remote/field sites: Where receiving happens outside the main warehouse.
- Third-party fulfillment/drop-ship: Where items never pass through central receiving.
If you have multiple business units, treat this as an enterprise standard with local procedures, not the other way around. Variance is where counterfeit and tampering risk hides.
What you actually need to do (step-by-step)
1) Define the “receipt validation gate”
Create a written procedure that states: no component is installed, connected, or imaged until SR-4(3) checks are completed and recorded. Tie the gate to a system record (asset ID, PO, shipment ID, or ticket).
Practical control design: Make the gate a required status in your procurement/asset workflow (for example: “Received → Quarantined/Staging → Validated → Ready for Deployment”).
2) Set the validation methods (your SR-4(3) parameter)
Because the control text is parameterized, you must choose and document methods that fit your supply chain. A workable baseline checklist:
A. Provenance and authorization checks
- Confirm the source is an approved third party (authorized reseller/distributor, manufacturer direct, or pre-approved marketplace listing).
- Match PO, part number/SKU, quantity, and expected country of origin (if tracked) to the shipment documents.
B. Packaging and tamper indicators
- Inspect seals, shrink-wrap, tamper-evident tape, and signs of reboxing.
- Photograph anomalies and record disposition.
C. Identifier verification
- Record serial numbers, device identifiers, and model numbers.
- Cross-check serial format or lookup with the manufacturer portal where available.
D. Technical integrity checks (where applicable)
- Validate software/firmware signatures or hashes provided by the publisher/manufacturer.
- For hardware appliances and images, validate checksums from a trusted channel and record the results.
- For devices that support secure boot/attestation, capture attestation evidence during staging.
You do not need every method for every component, but you do need a defined decision rule: which checks apply to which categories of components.
3) Assign ownership and escalation paths
SR-4(3) fails most often because everyone assumes someone else did the check.
Minimum ownership model:
- Control owner (GRC): defines procedure, trains stakeholders, monitors evidence completeness.
- Operational owner (Receiving/IT asset team): performs checks and records results.
- Security/IR contact: approves exceptions and runs investigation for suspected tampering.
- Procurement: enforces approved sourcing and blocks non-authorized purchases.
Define a simple escalation matrix:
- Fail (suspected tamper/counterfeit): quarantine item, open security incident, notify procurement, preserve packaging, stop deployment.
- Inconclusive: hold in quarantine, request manufacturer verification, require security approval before use.
- Pass: release to staging/deployment.
4) Integrate into intake workflows (make it hard to bypass)
Operationalize through systems you already use:
- Receiving logs (warehouse) + IT asset inventory (CMDB/ITAM) + ticketing (service desk).
- Require an attachment set (photos, checklist, hash verification output) before the ticket can move to “Ready for Deployment.”
Daydream fit (earned mention): If you manage many third parties and component types, Daydream can help you map SR-4(3) to a named control owner, a standard operating procedure, and a recurring evidence set so your team produces consistent audit-ready artifacts without rebuilding the workflow each assessment cycle.
5) Run sampling-based monitoring
You are proving operational effectiveness, not just design.
- Perform periodic spot checks that recent receipts have complete SR-4(3) evidence.
- Track exceptions and source them to root causes (drop-shipments, rush orders, remote sites, unauthorized suppliers).
Required evidence and artifacts to retain
Auditors will ask for records tied to real receipt events. Retain evidence in a retrievable system, linked to the asset or receiving ticket.
Core artifacts 1:
- Receiving checklist with pass/fail per control step and approver name.
- Purchase record: PO, supplier name, authorized channel confirmation.
- Shipment records: packing slip, tracking details, receiving date/time, receiver identity.
- Serial number capture and model verification record.
- Photos of packaging, seals, and labels (especially for exceptions).
- Hash/signature verification logs for software/firmware/images (screenshots are acceptable if logs are hard).
- Quarantine and disposition records for failed/inconclusive items.
- Exception approvals with rationale and compensating controls.
Program-level artifacts:
- SR-4(3) procedure and decision tree (which checks apply to which component categories).
- Roles and responsibilities (RACI) and training records for staff who receive/stage equipment.
- A list of approved sources/authorized third parties and how that list is maintained.
Common exam/audit questions and hangups
Expect questions like:
- “Show me three recent examples where you validated a component at receipt before deployment.”
- “How do you handle drop-shipped devices sent directly to remote employees?”
- “What checks apply to firmware updates and pre-built virtual appliances?”
- “Where is the evidence stored, and how do you ensure it can’t be altered after the fact?”
- “What triggers quarantine, and who can override it?”
Hangups that trigger deeper testing:
- Evidence exists only as a policy, not as per-receipt records.
- Checks rely on informal judgment (“it looked fine”) without criteria.
- Exceptions are frequent and not tracked to remediation.
Frequent implementation mistakes (and how to avoid them)
-
Mistake: treating SR-4(3) as a procurement-only control.
Fix: make receiving and staging accountable; procurement controls sourcing, but receiving controls acceptance. -
Mistake: no defined scope for “system component.”
Fix: publish categories (hardware, parts, software/firmware, images) and map required checks by category. -
Mistake: evidence lives in email threads.
Fix: force evidence into a ticket/asset record with required fields and attachments. -
Mistake: remote endpoints bypass intake.
Fix: ship to a controlled receiving location when possible; if not, require remote users/IT to complete a simplified validation checklist plus photos before onboarding. -
Mistake: no quarantine mechanism.
Fix: define a physical quarantine area for warehouses and a logical quarantine for images/software in a restricted repository.
Enforcement context and risk implications
No public enforcement cases were provided in the source catalog for SR-4(3), so this page does not cite enforcement actions.
Risk-wise, SR-4(3) is a control that reduces exposure to:
- Counterfeit components that fail early or behave unpredictably.
- Malicious modification (hardware/firmware/software) introduced before the asset ever reaches your network.
- Supply chain opacity that becomes a finding during federal assessments aligned to NIST SP 800-53. 2
A practical 30/60/90-day execution plan
First 30 days (Immediate stabilization)
- Assign a control owner and operational owner; publish a one-page SR-4(3) SOP.
- Define component categories and the minimum checks per category.
- Add a quarantine step to receiving/staging (physical location and ticket status).
- Update templates: receiving checklist, exception form, evidence naming convention.
By 60 days (Workflow integration)
- Integrate SR-4(3) into procurement and ITAM workflows (required fields and attachments).
- Train receiving teams, IT staging, and remote IT support on the checklist and escalation.
- Stand up an approved-source list process with procurement and security input.
- Start capturing hash/signature validation evidence for software/firmware intake.
By 90 days (Operational maturity)
- Run a short internal assessment: sample recent receipts, validate evidence completeness, document gaps.
- Reduce exceptions by addressing root causes (unauthorized purchasing paths, drop-ship process holes).
- Formalize metrics that matter operationally (exception volume, time in quarantine, missing evidence rate) and review them with owners.
- If you need repeatability across many third parties and receipt scenarios, configure Daydream to map SR-4(3) to owners, procedures, and recurring evidence requests, then track completion centrally.
Frequently Asked Questions
Does SR-4(3) apply to software downloads and cloud images, or only physical hardware?
It applies to “system or system component received,” which you should interpret to include software, firmware, and images you ingest into your environment. Define which integrity checks you require (hash/signature validation) and keep the verification output as evidence. 1
What’s the minimum acceptable validation if the manufacturer offers no attestation or signature tools?
Use compensating checks you can defend: authorized sourcing, packaging inspection, serial/part number verification, and quarantine plus enhanced testing before deployment. Document the decision rule so auditors see consistency rather than ad hoc judgment.
How do we handle drop-shipments to remote employees?
Require a remote intake checklist with photos of packaging, labels, and device identifiers, then record results in a ticket tied to the asset record. If you cannot validate adequately, route shipping through a controlled receiving site for higher-risk device types.
Can we sample receipts, or do we need to validate every component?
The control text focuses on validating received components, and assessment expectations usually favor evidence tied to actual receipt events. If you implement sampling for low-risk categories, document the rationale, sampling approach, and escalation rules, and be ready to defend it during an assessment. 2
What evidence do auditors ask for most often?
They typically ask for per-receipt proof: the checklist, serial capture, and integrity verification outputs where applicable, plus what you did with failed items. Program documents help, but they won’t substitute for transaction-level records.
Who should approve exceptions when validation is inconclusive?
Set a named approver role, usually security with procurement input, and require documented compensating controls (quarantine time, added testing, restricted deployment). Avoid letting receiving teams “override” based on schedule pressure.
Footnotes
Frequently Asked Questions
Does SR-4(3) apply to software downloads and cloud images, or only physical hardware?
It applies to “system or system component received,” which you should interpret to include software, firmware, and images you ingest into your environment. Define which integrity checks you require (hash/signature validation) and keep the verification output as evidence. (Source: NIST SP 800-53 Rev. 5 OSCAL JSON)
What’s the minimum acceptable validation if the manufacturer offers no attestation or signature tools?
Use compensating checks you can defend: authorized sourcing, packaging inspection, serial/part number verification, and quarantine plus enhanced testing before deployment. Document the decision rule so auditors see consistency rather than ad hoc judgment.
How do we handle drop-shipments to remote employees?
Require a remote intake checklist with photos of packaging, labels, and device identifiers, then record results in a ticket tied to the asset record. If you cannot validate adequately, route shipping through a controlled receiving site for higher-risk device types.
Can we sample receipts, or do we need to validate every component?
The control text focuses on validating received components, and assessment expectations usually favor evidence tied to actual receipt events. If you implement sampling for low-risk categories, document the rationale, sampling approach, and escalation rules, and be ready to defend it during an assessment. (Source: NIST SP 800-53 Rev. 5)
What evidence do auditors ask for most often?
They typically ask for per-receipt proof: the checklist, serial capture, and integrity verification outputs where applicable, plus what you did with failed items. Program documents help, but they won’t substitute for transaction-level records.
Who should approve exceptions when validation is inconclusive?
Set a named approver role, usually security with procurement input, and require documented compensating controls (quarantine time, added testing, restricted deployment). Avoid letting receiving teams “override” based on schedule pressure.
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