FDA Inspection 727293 — Frontida BioPharm LLC

Frontida BioPharm LLC — FEI 3004464206

The FDA completed an inspection of Frontida BioPharm LLC on May 20, 2011 in Philadelphia, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 20, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Philadelphia, PA (United States)