FDA Inspection 631886 — Catalent Greenville Inc
The FDA completed an inspection of Catalent Greenville Inc on Nov 13, 2009 in Greenville, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Nov 13, 2009
- Fiscal Year
- 2010
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Greenville, NC (United States)