FDA inspection
Sidmak Laboratories India Pvt Ltd: FDA inspection ending Oct 26, 2012
FDA inspection 806835 · Voluntary Action Indicated (VAI) · Dehradun
Key facts
| Inspection ID | 806835 |
|---|---|
| Firm | Sidmak Laboratories India Pvt Ltd |
| FEI number | 3008127341 |
| Address | Plot No. 20 Pharma City, Selaqui Ind. Area, Vikas Nagar |
| City | Dehradun |
| Country | India |
| Fiscal year | 2013 |
| Inspection end date | Oct 26, 2012 |
| 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