FDA Inspection
dorsaVi LtddorsaVi Ltd – FDA Inspection, Oct 29, 2015
Record Details
This FDA Inspection record concerns dorsaVi Ltd, with an inspection on October 29, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- dorsaVi Ltd
- Inspection Date
- October 29, 2015
- Product Type
- Devices
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ID · 07558d64-2b4a-4776-99aa-1b6ae62fb98c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 949099
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.86Acceptance status
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