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FDA Inspection 961359 — Frontida Biopharm, LLC

Frontida Biopharm, LLC — FEI 3008087151

The FDA completed an inspection of Frontida Biopharm, LLC on February 18, 2016 in Aurora, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 18, 2016
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Aurora, IL (United States)

Facility

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FDA data resources