FDA Inspection
Pro-Med Instruments GmbhPro-Med Instruments Gmbh – FDA Inspection, Nov 6, 2014
Record Details
This FDA Inspection record concerns Pro-Med Instruments Gmbh, with an inspection on November 6, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Pro-Med Instruments Gmbh
- Inspection Date
- November 6, 2014
- Product Type
- Devices
View Company Profile
ID · 91f70049-e14c-404f-80e1-c7b5e6359744
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 905154
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Pro-Med Instruments Gmbh
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 22, 2017 | Not classified | Office of Inspections and Investigations | Compliance: Devices |
| June 21, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Pro-Med Instruments Gmbh
- FDA Inspection 1015579 - 2017-06-22
- FDA Inspection 790986 - 2012-06-21
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