FDA inspection
Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.: FDA inspection ending Mar 24, 2017
FDA inspection 1007608 · Official Action Indicated (OAI) · Saint Louis, MO
Key facts
| Inspection ID | 1007608 |
|---|---|
| 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 | 2017 |
| Inspection end date | Mar 24, 2017 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 525881 |
At a glance
- 10–99 Citations
- 1–9 Posted citations
- Yes 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