FDA Inspection
Morgan Medesign, Inc.Morgan Medesign, Inc. – FDA Inspection, Jun 18, 2013
Record Details
This FDA Inspection record concerns Morgan Medesign, Inc., with an inspection on June 18, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Morgan Medesign, Inc.
- Inspection Date
- June 18, 2013
- Product Type
- Devices
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ID · 9af479db-3154-46dd-b211-f774ac2ce390
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 835639
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.22Quality Audits - defined intervals
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Other FDA inspections of Morgan Medesign, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 29, 2016 | 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 985831 - 2016-03-29
- FDA Inspection 618335 - 2009-09-25
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