FDA Inspection
BTG International GermanyBTG International Germany – FDA Inspection, Mar 17, 2016
Record Details
This FDA Inspection record concerns BTG International Germany, with an inspection on March 17, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- BTG International Germany
- Inspection Date
- March 17, 2016
- Product Type
- Devices
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ID · a55e3625-1d13-4ad5-8b78-24447cdcc938
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 965692
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.250(a)Statistical techniques - Lack of or inadequate procedures
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