FDA Inspection 546751 — AmbioPharm, Inc
The FDA completed an inspection of AmbioPharm, Inc on November 4, 2008 in Beech Island, SC. 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
- November 4, 2008
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Beech Island, SC (United States)