# FDA Inspection 1025556 - OmniLife Science - September 13, 2017

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

> FDA Inspection 1025556 for OmniLife Science on September 13, 2017. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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