FDA Inspection
Accumedix, Inc.Accumedix, Inc. – FDA Inspection, Dec 5, 2011
Record Details
This FDA Inspection record concerns Accumedix, Inc., with an inspection on December 5, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Accumedix, Inc.
- Inspection Date
- December 5, 2011
- Product Type
- Devices
View Company Profile
ID · 8f8f22e4-e78e-4865-9b3a-6ac8fe682f58
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 756447
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Accumedix, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 17, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 6, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 19, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Accumedix, Inc.
- FDA Inspection 985551 - 2016-08-17
- FDA Inspection 846362 - 2013-08-06
- FDA Inspection 678206 - 2010-08-19
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