FDA Inspection
Microfit, Inc.Microfit, Inc. – FDA Inspection, Nov 9, 2011
Record Details
This FDA Inspection record concerns Microfit, Inc., with an inspection on November 9, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Microfit, Inc.
- Inspection Date
- November 9, 2011
- Product Type
- Devices
View Company Profile
ID · 40f6d680-f79f-4450-9582-cf61743a3201
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 752333
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 806.20(b)(3)Events
- 21 CFR 820.50(a)(1)Evaluation and Selection, Suppliers, Contractors, etc.
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.250(b)Sampling methods - Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Microfit, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 24, 2023 | Not classified | San Francisco District Office | |
| August 20, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 27, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Microfit, Inc.
- FDA Inspection 1208583 - 2023-05-24
- FDA Inspection 1063445 - 2018-08-20
- FDA Inspection 927254 - 2015-05-27
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