FDA Inspection
Omni Surgical LpOmni Surgical Lp – FDA Inspection, Mar 29, 2010
Record Details
This FDA Inspection record concerns Omni Surgical Lp, with an inspection on March 29, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Omni Surgical Lp
- Inspection Date
- March 29, 2010
- Product Type
- Devices
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ID · 1dfbf537-645a-4f9d-b277-bd51fb5bfdf7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 654088
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 803.50(a)(2)Individual Report of Malfunction
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Other FDA inspections of Omni Surgical Lp
1| Date | Classification | Office | Project area |
|---|---|---|---|
| October 26, 2010 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Omni Surgical Lp
- FDA Inspection 696640 - 2010-10-26
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