FDA Inspection
Gardner Denver Thomas, IncGardner Denver Thomas, Inc – FDA Inspection, Oct 31, 2011
Record Details
This FDA Inspection record concerns Gardner Denver Thomas, Inc, with an inspection on October 31, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Gardner Denver Thomas, Inc
- Inspection Date
- October 31, 2011
- Product Type
- Devices
View Company Profile
ID · 5b64c610-9d2f-4acf-9864-a982e584c538
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 752076
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 803.17(a)(2)Lack of System for Determining MDR Events
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Other FDA inspections of Gardner Denver Thomas, Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 22, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Gardner Denver Thomas, Inc
- FDA Inspection 928436 - 2015-05-22
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