FDA inspection
Aarti Pharmalabs Limited (Custom Synthesis Division): FDA inspection ending Oct 1, 2009
FDA inspection 619163 · Voluntary Action Indicated (VAI) · Vapi, Valsad
Key facts
| Inspection ID | 619163 |
|---|---|
| Firm | Aarti Pharmalabs Limited (Custom Synthesis Division) |
| FEI number | 3007850324 |
| Address | Custom Synthesis Division, Plot 22c/1, Phase 1, Gidc Estate |
| City | Vapi, Valsad |
| Country | India |
| Fiscal year | 2010 |
| Inspection end date | Oct 1, 2009 |
| 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