Compliance document
Form FDA 483: Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.
FDA FOIA
Key facts
| Document type | Form FDA 483 |
|---|---|
| Firm | Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. |
| FEI number | 1950222 |
| Inspection | 230826 |
| Collection | FDA FOIA |
At a glance
- 10–99 Pages
- 10–99 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspection and compliance documents
The Orca1 document library indexes FDA compliance documents such as Form 483 observations, establishment inspection reports and firm responses. Documents are available to Orca1 subscribers only.
Source: U.S. Food and Drug Administration (FDA) records, Orca1 document library