FDA Inspection
LGC Clinical Diagnostics, Inc.LGC Clinical Diagnostics, Inc. – FDA Inspection, Jun 28, 2011
Record Details
This FDA Inspection record concerns LGC Clinical Diagnostics, Inc., with an inspection on June 28, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 28, 2011
- Product Type
- Devices
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ID · bdd9c2b2-bb9e-4fb2-b28b-2ef5ec395d27
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 733038
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of LGC Clinical Diagnostics, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 10, 2025 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 11, 2018 | Not classified | New England District Office | |
| March 28, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for LGC Clinical Diagnostics, Inc.
- FDA Inspection 1297464 - 2025-12-10
- FDA Inspection 1120150 - 2018-10-11
- FDA Inspection 775644 - 2012-03-28
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