# FDA Inspection 654088 - Omni Surgical Lp - March 29, 2010

Source: https://www.keypedia.com/records/fda_inspections/omni-surgical-lp/1dfbf537-645a-4f9d-b277-bd51fb5bfdf7
Source feed: FDA_Inspections

> FDA Inspection 654088 for Omni Surgical Lp on March 29, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 654088
- Company Name: Omni Surgical Lp
- Inspection Date: 2010-03-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 696640 - 2010-10-26](https://www.keypedia.com/records/fda_inspections/omni-surgical-lp/79769373-1e38-4ff0-bc5a-f794dbbd17b4)

Company: https://www.keypedia.com/companies/omni-surgical-lp/9076ab13-a935-4420-8644-ecc520f60cd9

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7