FDA inspection
Vimta Labs Limited: FDA inspection ending May 13, 2019
FDA inspection 1090966 · Voluntary Action Indicated (VAI) · Hyderabad
Key facts
| Inspection ID | 1090966 |
|---|---|
| Firm | Vimta Labs Limited |
| FEI number | 3006587427 |
| Address | Genome Valley, 5 Mn Shamirpet |
| City | Hyderabad |
| Country | India |
| Fiscal year | 2019 |
| Inspection end date | May 13, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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