FDA Inspection
Gardner Denver Thomas IncGardner Denver Thomas Inc – FDA Inspection, Feb 6, 2015
Record Details
This FDA Inspection record concerns Gardner Denver Thomas Inc, with an inspection on February 6, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Gardner Denver Thomas Inc
- Inspection Date
- February 6, 2015
- Product Type
- Devices
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ID · 397e362f-0f05-46a4-bd62-5a8c8e55d17f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 913129
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 806.20(b)(4)Justification for not reporting
- 21 CFR 820.72(b)Calibration procedures - content
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Other FDA inspections of Gardner Denver Thomas Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 3, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Gardner Denver Thomas Inc
- FDA Inspection 737266 - 2011-08-03
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