FDA Inspection 961359 — Frontida Biopharm, LLC
The FDA completed an inspection of Frontida Biopharm, LLC on Feb 18, 2016 in Aurora, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 18, 2016
- Fiscal Year
- 2016
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Aurora, IL (United States)