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 3008087151.
Observations4
Issue DateOctober 24, 2025
StatusNo Warning Letter
Related Inspections6
Establishment Details
Firm
Frontida Biopharm, LLC
Location
Aurora, Illinois
FEI Number
3008087151
Product Type
Drugs
Issue Date
October 24, 2025
Country
United States
Inspection History, 2010 to 2025
NAI5
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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