FDA Inspection
Anchor Products Company, Inc.Anchor Products Company, Inc. – FDA Inspection, Oct 25, 2013
Record Details
This FDA Inspection record concerns Anchor Products Company, Inc., with an inspection on October 25, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- October 25, 2013
- Product Type
- Devices
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ID · f59a260f-1a9a-4ba8-adcd-bc9b6878baec
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 854186
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 803.50(a)(2)Individual Report of Malfunction
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of Anchor Products Company, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 26, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 12, 2011 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 4, 2010 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Anchor Products Company, Inc.
- FDA Inspection 985552 - 2016-09-26
- FDA Inspection 725032 - 2011-05-12
- FDA Inspection 666324 - 2010-06-04
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