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FDA Inspection 713580 — OmniLife Science

OmniLife Science — FEI 3008342029

The FDA completed an inspection of OmniLife Science on February 3, 2011 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
February 3, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Raynham, MA (United States)

Facility

Other inspections at this facility

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  • 1025556 (NAI Wed Sep 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 810557 (VAI Thu Dec 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources