FDA inspection
Ajanta Pharma Limited: FDA inspection ending Jun 22, 2019
FDA inspection 1098820 · Voluntary Action Indicated (VAI) · Bharuch
Key facts
| Inspection ID | 1098820 |
|---|---|
| Firm | Ajanta Pharma Limited |
| FEI number | 3012664809 |
| Address | Plot No Z-103 /A Dahej Sez - Part Ii |
| City | Bharuch |
| Country | India |
| Fiscal year | 2019 |
| Inspection end date | Jun 22, 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
- 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