FDA inspection
Glenmark Pharmaceuticals Limited: FDA inspection ending Nov 11, 2017
FDA inspection 1031652 · Voluntary Action Indicated (VAI) · Solan
Key facts
| Inspection ID | 1031652 |
|---|---|
| Firm | Glenmark Pharmaceuticals Limited |
| FEI number | 3005757050 |
| Address | Village Kishanpura, Baddi Nalagarh Road, Baddi |
| City | Solan |
| Country | India |
| Fiscal year | 2018 |
| Inspection end date | Nov 11, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| 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