FDA inspection
Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.: FDA inspection ending Mar 23, 2015
FDA inspection 919720 · Voluntary Action Indicated (VAI) · Saint Louis, MO
Key facts
| Inspection ID | 919720 |
|---|---|
| Firm | Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. |
| FEI number | 1950222 |
| Address | 2555 Hermelin Dr. |
| City | Saint Louis |
| State | MO |
| ZIP | 63146 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Mar 23, 2015 |
| 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
- 10–99 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