FDA Inspection
MEDIA PLUS, LLCMEDIA PLUS, LLC – FDA Inspection, Mar 10, 2023
Record Details
This FDA Inspection record concerns MEDIA PLUS, LLC, with an inspection on March 10, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d82218b6-cb5d-4408-9e82-8dd23e1938fe
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1199594
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 820.184Lack of or inadequate DHR procedures
- 21 CFR 820.20(c)Management review dates
- 21 CFR 820.22Quality Audits - defined intervals
- 21 CFR 820.30(a)Design control - no procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of MEDIA PLUS, LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 27, 2025 | NAI | Compliance: Devices |
Other documents for MEDIA PLUS, LLC
- FDA Inspection 1259446 - 2025-01-27
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