FDA inspection
Catalent Maryland, Inc.: FDA inspection ending Nov 4, 2019
FDA inspection 1112131 · Voluntary Action Indicated (VAI) · Baltimore, MD
Key facts
| Inspection ID | 1112131 |
|---|---|
| Firm | Catalent Maryland, Inc. |
| FEI number | 3015558590 |
| Address | 801 W Baltimore St Ste 302 |
| City | Baltimore |
| State | MD |
| ZIP | 21201 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Nov 4, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 1–9 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