# OmniLife Science – FDA Inspection, Sep 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/omnilife-science/da50428d-f169-4058-abb9-f420c7873db6
Source feed: FDA_Inspections

> FDA inspection 1025556 of OmniLife Science, September 13, 2017. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025556
- Company Name: OmniLife Science
- Inspection Date: 2017-09-13
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1166323 - 2022-04-04](https://www.keypedia.com/records/fda_inspections/omnilife-science/cb59476c-a3d4-448c-be77-e133b5d72249)
- [FDA Inspection 810557 - 2012-12-06](https://www.keypedia.com/records/fda_inspections/omnilife-science/11c66961-2553-46b3-819c-390794de3f8a)
- FDA Inspection 713580 - 2011-02-03

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

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