FDA Inspection
Gregory Manufacturing, Inc.Gregory Manufacturing, Inc. – FDA Inspection, Sep 12, 2014
Record Details
This FDA Inspection record concerns Gregory Manufacturing, Inc., with an inspection on September 12, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Gregory Manufacturing, Inc.
- Inspection Date
- September 12, 2014
- Product Type
- Devices
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ID · 132bbec8-db4a-44fd-ac7a-8b46ff2f1bee
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 896691
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.184Lack of or inadequate DHR procedures
- 21 CFR 820.70(a)Production processes
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Other FDA inspections of Gregory Manufacturing, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| April 2, 2026 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 21, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 21, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Gregory Manufacturing, Inc.
- FDA Inspection 1311716 - 2026-04-02
- FDA Inspection 1075004 - 2018-11-21
- FDA Inspection 747165 - 2011-09-21
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