Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3008342029.
Observations2
Issue DateSeptember 13, 2017
StatusNo Warning Letter
Related Inspections4
Establishment Details
Firm
OmniLife Science
Location
Raynham, Massachusetts, United States
FEI Number
3008342029
Product Type
Devices
Issue Date
September 13, 2017
Country
United States
Inspection History, 2011 to 2022
NAI2
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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