# OmniLife Science – FDA Inspection, Dec 6, 2012

Source: https://www.keypedia.com/records/fda_inspections/omnilife-science/11c66961-2553-46b3-819c-390794de3f8a
Source feed: FDA_Inspections

> FDA inspection 810557 of OmniLife Science, December 06, 2012. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 810557
- Company Name: OmniLife Science
- Inspection Date: 2012-12-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

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Company: https://www.keypedia.com/companies/omnilife-science/1b8099a5-df71-4f4d-96b0-f0937f348d11

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