FDA Inspection
Alfa Medical Specialist IncAlfa Medical Specialist Inc – FDA Inspection, Nov 20, 2009
Record Details
This FDA Inspection record concerns Alfa Medical Specialist Inc, with an inspection on November 20, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Alfa Medical Specialist Inc
- Inspection Date
- November 20, 2009
- Product Type
- Devices
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ID · 695db247-cb7a-432f-ae5c-a1d38a527590
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 630587
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of Alfa Medical Specialist Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 12, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Alfa Medical Specialist Inc
- FDA Inspection 791775 - 2012-07-12
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