FDA Inspection
Biomet UK Ltd.Biomet UK Ltd. – FDA Inspection, Mar 18, 2015
Record Details
This FDA Inspection record concerns Biomet UK Ltd., with an inspection on March 18, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Biomet UK Ltd.
- Inspection Date
- March 18, 2015
- Product Type
- Devices
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ID · 3d51f05b-b53d-4b91-9606-3f38956b203c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 918189
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
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Other FDA inspections of Biomet UK Ltd.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 2, 2023 | Not classified | Office of Inspections and Investigations | |
| August 3, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 2, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Biomet UK Ltd.
- FDA Inspection 1222658 - 2023-11-02
- FDA Inspection 1021429 - 2017-08-03
- FDA Inspection 596100 - 2009-07-02
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