FDA 21 CFR 820.184 Device History Record DHR Completeness Audit
This checklist covers FDA 21 CFR 820.184 Device History Record DHR Completeness Audit requirements under applicable federal and industry regulations. Violations may result in civil penalties up to $15,625 per violation per day and potential operational suspension.
- Industry: Healthcare
- Frequency: Quarterly
- Estimated Time: 20-30 minutes
- Role: QA Manager
- Total Items: 20
- Compliance: 21 CFR Part 820, ISO 13485, FDA QSR
Regulatory Documentation & Compliance Status
Verify current regulatory compliance status and required documentation is in order.
- Are all applicable permits, licenses, and registrations current and posted?
- Has required training been completed and documented for all personnel assigned to this area?
- Are all required safety signs, labels, and warnings in place and legible?
- Attach photo of permit postings and safety signage:
Safety Equipment & Inspection Records
Verify safety equipment condition and inspection record currency.
- Are all required safety inspections current and documented?
- Is personal protective equipment available, maintained, and used correctly?
- Number of open deficiencies from previous inspection:
- Attach photo of safety equipment and inspection records:
Work Practices & Housekeeping
Evaluate worker compliance with safe work practices and housekeeping standards.
- Are workers following established safe work procedures and using required PPE?
- Is housekeeping adequate with no trip hazards, blocked egress, or unsecured materials?
- Work area safety and housekeeping assessment:
- Attach photo of work area conditions and housekeeping:
Previous Findings Review & Supervisor Certification
Review prior findings and obtain supervisor acknowledgment of current inspection.
- Have all findings from previous inspections been corrected and verified effective?
- Is supervision aware of all current compliance issues and engaged in resolution?
- Total corrective actions assigned from this inspection:
- Responsible supervisor or area lead certification of inspection:
Corrective Actions & Inspector Sign-Off
Document all deficiencies and assign corrective actions. POPProbe auto-assigns these to team members, generates a signed PDF report instantly, and tracks compliance status across all locations. -> Start free, no credit card required
- List all deficiencies identified in this inspection:
- Overall compliance status?
- Corrective actions assigned to (name and department):
- Inspector digital signature and date:
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Why Use This FDA 21 CFR 820.184 Device History Record DHR Completeness Audit?
This fda 21 cfr 820.184 device history record dhr completeness audit helps healthcare teams maintain compliance and operational excellence. Designed for qa manager professionals, this checklist covers 20 critical inspection points across 5 sections. Recommended frequency: quarterly.
Ensures compliance with 21 CFR Part 820, ISO 13485, FDA QSR. Regulatory-aligned for audit readiness and inspection documentation.
Frequently Asked Questions
What does the FDA 21 CFR 820.184 Device History Record DHR Completeness Audit cover?
This checklist covers 20 inspection items across 5 sections: Regulatory Documentation & Compliance Status, Safety Equipment & Inspection Records, Work Practices & Housekeeping, Previous Findings Review & Supervisor Certification, Corrective Actions & Inspector Sign-Off. It is designed for healthcare operations and compliance.
How often should this checklist be completed?
This checklist should be completed quarterly. Each completion takes approximately 20-30 minutes.
Who should use this FDA 21 CFR 820.184 Device History Record DHR Completeness Audit?
This checklist is designed for QA Manager professionals in the healthcare industry. It can be used for self-assessments, team audits, and regulatory compliance documentation.
Can I download this checklist as a PDF?
Yes, this checklist is available as a free PDF download. You can also use it digitally in the POPProbe mobile app for real-time data capture, photo documentation, and automatic reporting.