FDA inspection
Catalent Greenville Inc: FDA inspection ending Apr 13, 2017
FDA inspection 1019260 · No Action Indicated (NAI) · Greenville, NC
Key facts
| Inspection ID | 1019260 |
|---|---|
| Firm | Catalent Greenville Inc |
| FEI number | 3000209735 |
| Address | 1240 Sugg Pkwy |
| City | Greenville |
| State | NC |
| ZIP | 27834 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Apr 13, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data