FDA inspection
Gensynth Laboratories Private Limited: FDA inspection ending Sep 21, 2017
FDA inspection 1030256 · No Action Indicated (NAI) · Sangareddy District, Medak
Key facts
| Inspection ID | 1030256 |
|---|---|
| Firm | Gensynth Laboratories Private Limited |
| FEI number | 3008800173 |
| Address | & 239 Plot 220 |
| City | Sangareddy District, Medak |
| Country | India |
| Fiscal year | 2017 |
| Inspection end date | Sep 21, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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