FDA Inspection
DMG America LLC dba Goldsmith & Revere, Inc.DMG America LLC dba Goldsmith & Revere, Inc. – FDA Inspection, Jul 7, 2010
Record Details
This FDA Inspection record concerns DMG America LLC dba Goldsmith & Revere, Inc., with an inspection on July 7, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 7, 2010
- Product Type
- Devices
View Company Profile
ID · a604f4a9-ba0c-4da9-9cb1-3e6f819c6e56
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 670226
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
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 |
| March 20, 2012 | VAI | Center for Devices and Radiological Health | Compliance: 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 770501 - 2012-03-20
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