FDA Inspection 781692 — Catalent Greenville Inc
The FDA completed an inspection of Catalent Greenville Inc on May 11, 2012 in Greenville, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- May 11, 2012
- Fiscal Year
- 2012
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Greenville, NC (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3565 | 21 CFR 211.58 | Buildings not maintained in good state of repair |