FDA Inspection
Morgan Medesign, Inc.Morgan Medesign, Inc. – FDA Inspection, Mar 29, 2016
Record Details
This FDA Inspection record concerns Morgan Medesign, Inc., with an inspection on March 29, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Morgan Medesign, Inc.
- Inspection Date
- March 29, 2016
- Product Type
- Devices
View Company Profile
ID · 501f3fdc-6d27-4ae3-a29e-f4715fee3afc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 985831
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.80(e)Documentation
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Morgan Medesign, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 18, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 25, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Morgan Medesign, Inc.
- FDA Inspection 835639 - 2013-06-18
- FDA Inspection 618335 - 2009-09-25
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