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FDA Inspection
•Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.•February 21, 2014

Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. – FDA Inspection, Feb 21, 2014

Record Details

This FDA Inspection record concerns Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P., with an inspection on February 21, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.
Inspection Date
February 21, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · bc3bb460-5e65-44d9-a785-6b5463eaca0f

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
869584
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.

19
DateClassificationOfficeProject area
June 30, 2026Not classifiedKansas City District OfficeCompliance: Devices
June 5, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 21, 2019OAICenter for Devices and Radiological HealthCompliance: Devices
June 6, 2019Not classifiedKansas City District OfficeCompliance: Devices
March 24, 2017OAICenter for Devices and Radiological HealthCompliance: Devices
View all 19 other inspections on the company page
Other documents for Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P.
  • FDA Inspection 1324912 - 2026-06-30
  • FDA Inspection 1237960 - 2024-06-05
  • FDA Inspection 1113441 - 2019-12-21
  • FDA Inspection 1092063 - 2019-06-06
  • FDA Inspection 1007608 - 2017-03-24

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