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 1815703.
Observations3
Issue DateOctober 16, 2025
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
Liquipak Corporation
Location
Alma, Michigan, United States
FEI Number
1815703
Product Type
Drugs
Issue Date
October 16, 2025
Country
United States
Inspection History, 2013 to 2025
NAI1
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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