FDA Inspection
Volker GmBHVolker GmBH – FDA Inspection, Feb 26, 2015
Record Details
This FDA Inspection record concerns Volker GmBH, with an inspection on February 26, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Volker GmBH
- Inspection Date
- February 26, 2015
- Product Type
- Devices
View Company Profile
ID · bfe9bdc0-9bd9-48dd-8428-04e16bd68aff
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 918030
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.198(a)Complaints
- 21 CFR 820.250(b)Sampling plans
- 21 CFR 820.184DHR content
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Volker GmBH
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 27, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Volker GmBH
- FDA Inspection 803968 - 2012-09-27
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