FDA inspection
Glenmark Pharmaceuticals Inc USA: FDA inspection ending May 18, 2018
FDA inspection 1052635 · Voluntary Action Indicated (VAI) · Monroe, NC
Key facts
| Inspection ID | 1052635 |
|---|---|
| Firm | Glenmark Pharmaceuticals Inc USA |
| FEI number | 3011585599 |
| Address | 4147 Goldmine Rd |
| City | Monroe |
| State | NC |
| ZIP | 28110-7759 |
| Fiscal year | 2018 |
| Inspection end date | May 18, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Generic Drug Evaluation |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No 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