FDA inspection
Kindeva Drug Delivery LP: FDA inspection ending May 18, 2006
FDA inspection 426738 · No Action Indicated (NAI) · Saint Paul, MN
Key facts
| Inspection ID | 426738 |
|---|---|
| Firm | Kindeva Drug Delivery LP |
| FEI number | 3003803251 |
| Address | 42 Water St W Bldg 75 |
| City | Saint Paul |
| State | MN |
| ZIP | 55107-2009 |
| Fiscal year | 2006 |
| Inspection end date | May 18, 2006 |
| Classification | No Action Indicated (NAI) |
| Project area | Generic Drug Evaluation |
| Product type | Drugs |
At a glance
- None Citations
- None 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