FDA Inspection
DMG America LLC dba Goldsmith & Revere, Inc.DMG America LLC dba Goldsmith & Revere, Inc. – FDA Inspection, Mar 20, 2012
Record Details
This FDA Inspection record concerns DMG America LLC dba Goldsmith & Revere, Inc., with an inspection on March 20, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 20, 2012
- Product Type
- Devices
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ID · b2ae5255-6830-42da-9494-589a8ed6c7b3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 770501
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.20(b)Lack of or inadequate organizational structure
Full citation text and observation details available on the Dashboard.
Other FDA inspections of DMG America LLC dba Goldsmith & Revere, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| November 12, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 13, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 29, 2013 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 7, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for DMG America LLC dba Goldsmith & Revere, Inc.
- FDA Inspection 951941 - 2015-11-12
- FDA Inspection 854944 - 2013-11-13
- FDA Inspection 816472 - 2013-01-29
- FDA Inspection 670226 - 2010-07-07
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