FDA Inspection 1166323 — OmniLife Science

OmniLife Science — FEI 3008342029

The FDA completed an inspection of OmniLife Science on April 4, 2022 in Raynham, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 4, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Raynham, MA (United States)