FDA inspection
Cadila Healthcare Limited (Zyfine): FDA inspection ending Nov 6, 2008
FDA inspection 554444 · Voluntary Action Indicated (VAI) · Ahmedabad
Key facts
| Inspection ID | 554444 |
|---|---|
| Firm | Cadila Healthcare Limited (Zyfine) |
| FEI number | 3006595385 |
| Address | 266 267 Sur 265, Sarkhej - Bavla Nh 8a |
| City | Ahmedabad |
| Fiscal year | 2009 |
| Inspection end date | Nov 6, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Generic Drug Evaluation |
| 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