FDA Inspection
Owen Mumford USA, Inc.FDA Inspection 904740 - Owen Mumford USA, Inc. - October 31, 2014
Record Details
This FDA Inspection record concerns Owen Mumford USA, Inc., with an inspection on October 31, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Owen Mumford USA, Inc.
- Inspection Date
- October 31, 2014
- Product Type
- Devices
View Company Profile
ID · d78d2248-0dbd-4459-b2b3-48cb307636f2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 904740
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(b)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Owen Mumford USA, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 5, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 12, 2013 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 10, 2011 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Owen Mumford USA, Inc.
- FDA Inspection 1098838 - 2019-03-05
- FDA Inspection 859742 - 2013-12-12
- FDA Inspection 740437 - 2011-08-10
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