FDA Inspection
taberna pro medicumtaberna pro medicum – FDA Inspection, Nov 1, 2012
Record Details
This FDA Inspection record concerns taberna pro medicum, with an inspection on November 1, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- taberna pro medicum
- Inspection Date
- November 1, 2012
- Product Type
- Devices
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ID · 590eb90a-1b85-4821-a5ae-81096fd48e54
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 808669
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.22Quality audits - auditor independence
- 21 CFR 820.30(f)Design verification - Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.184DHR content
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Other FDA inspections of taberna pro medicum
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 14, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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