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  5. Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P., Saint Louis, MO – FDA Inspections
Company
•United States

Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P., Saint Louis, MO – FDA Inspections

Inspection records and compliance data for Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. in Saint Louis, Missouri. 20 FDA inspections on record (9 OAI), 3 Form 483s, 1 warning letter, last inspected June 30, 2026.

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Company Profile

This profile covers Meridian Medical Technologies, LLC a Subsidiary of Kindeva Drug Delivery, L.P. based in Saint Louis, Missouri, United States.

FDA Inspection History

FDA inspections
20
OAI
9
VAI
8
NAI
1
Unclassified
2
Form 483s
3
Warning letters
1

First inspected July 31, 2009. Last inspected June 30, 2026.

Most cited issue areas

  • Procedures for sterile drug products8 inspections
  • Control procedures to monitor and validate performance5 inspections
  • Investigations of discrepancies, failures5 inspections

FDA inspections (20)

DateResultFDA center(s)Insp. #
June 30, 2026Not classifiedMedical Devices & Rad Health · Compliance: Devices1324912
June 5, 2024VAIHuman Drugs, Medical Devices & Rad Health · Drug Quality Assurance1237960
December 21, 2019OAIHuman Drugs, Medical Devices & Rad Health · Compliance: Devices1113441
June 6, 2019Not classifiedHuman Drugs, Medical Devices & Rad Health · Compliance: Devices1092063
March 24, 2017OAIHuman Drugs, Medical Devices & Rad Health · Compliance: Devices1007608
March 23, 2015VAIHuman Drugs · Drug Quality Assurance919720
November 25, 2014OAIHuman Drugs, Medical Devices & Rad Health · Compliance: Devices902281
February 21, 2014OAIHuman Drugs, Medical Devices & Rad Health · Drug Quality Assurance869584
February 21, 2014OAIHuman Drugs, Medical Devices & Rad Health · Compliance: Devices867214
October 9, 2013OAIHuman Drugs · Drug Quality Assurance851640
October 9, 2013OAIHuman Drugs · Drug Quality Assurance851436
April 29, 2013OAIHuman Drugs · Drug Quality Assurance824746
March 4, 2013OAIHuman Drugs, Medical Devices & Rad Health · Drug Quality Assurance821534
February 13, 2012VAIHuman Drugs · Drug Quality Assurance769019
February 13, 2012VAIHuman Drugs · Drug Quality Assurance767484
May 12, 2011NAIHuman Drugs · Drug Quality Assurance725261
August 18, 2010VAIHuman Drugs · Drug Quality Assurance676197
August 18, 2010VAIHuman Drugs · Drug Quality Assurance676196
July 31, 2009VAIHuman Drugs · Drug Quality Assurance598495
July 31, 2009VAIHuman Drugs · Bioresearch Monitoring598493
FDA documents

Form 483s (6)

  • Form 483s · December 21, 2019
  • Form 483s · March 24, 2017
  • Form 483s · February 21, 2014
  • Form 483s · March 4, 2013
  • Form 483s · February 13, 2012
  • Form 483s · June 13, 2008

Warning Letters (1)

  • Warning Letters · March 24, 2017
People (5)
Veronica L. Call
Person
Shirley J. Berryman
Person
Sandra A. Hughes
Person
Michele L. Obert
Person
Kellia N. Hicks
Person
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Company Information

Name

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

FEI Number

1950222

Address

1945 Craig Rd, Saint Louis, Missouri 63146, United States

Country

United States

ID: 00b844de-fb09-432d-96ab-31b8f7192a5d

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Contact
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Scranton Office:
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🇪🇺+48 532-447-507
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