FDA Inspection
Medifix, Inc.Medifix, Inc. – FDA Inspection, Oct 15, 2009
Record Details
This FDA Inspection record concerns Medifix, Inc., with an inspection on October 15, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medifix, Inc.
- Inspection Date
- October 15, 2009
- Product Type
- Devices
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ID · ebae72e2-7554-4c60-9029-5f2f2ee6570d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 621631
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.22Quality Audit/Reaudit - conducted
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Other FDA inspections of Medifix, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 8, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 18, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Medifix, Inc.
- FDA Inspection 1026647 - 2017-08-08
- FDA Inspection 822164 - 2013-03-18
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