FDA Inspection
Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. – FDA Inspection, Jul 31, 2009
Record Details
This FDA Inspection record concerns Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P., with an inspection on July 31, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- July 31, 2009
- Product Type
- Drugs
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ID · b776aed6-ebc8-413e-b799-db19a31ed523
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 598493
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 211.113(b)Procedures for sterile drug products
- 21 CFR 211.182Personnel dating/signing equipment log
- 21 CFR 211.100(b)SOPs not followed / documented
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Other FDA inspections of Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.
19| Date | Classification | Office | Project area |
|---|---|---|---|
| June 30, 2026 | Not classified | Kansas City District Office | Compliance: Devices |
| June 5, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 21, 2019 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 6, 2019 | Not classified | Kansas City District Office | Compliance: Devices |
| March 24, 2017 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
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