FDA Inspection
Mossman Associates, Inc.Mossman Associates, Inc. – FDA Inspection, Aug 29, 2018
Record Details
This FDA Inspection record concerns Mossman Associates, Inc., with an inspection on August 29, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 24200e3b-07fc-4f1a-80be-6ccaab7c743f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1063734
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of Mossman Associates, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 16, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 9, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Mossman Associates, Inc.
- FDA Inspection 814982 - 2013-01-16
- FDA Inspection 633081 - 2009-12-09
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