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•United States

KP Pharmaceutical Technology, Bloomington, IN – FDA Inspections

Inspection records and compliance data for KP Pharmaceutical Technology in Bloomington, Indiana. 8 FDA inspections on record (2 OAI), 2 Form 483s, last inspected February 13, 2026.

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Company Profile

This profile covers KP Pharmaceutical Technology based in Bloomington, Indiana, United States.

FDA Inspection History

FDA inspections
8
OAI
2
VAI
3
NAI
2
Unclassified
1
Form 483s
2
Warning letters
0

First inspected September 22, 2009. Last inspected February 13, 2026.

Most cited issue areas

  • Procedures for sterile drug products2 inspections
  • Aseptic Processing Area1 inspection
  • Cleaning System1 inspection

FDA inspections (8)

DateResultFDA center(s)Insp. #
February 13, 2026Not classifiedHuman Drugs1307874
March 21, 2024OAIHuman Drugs · Drug Quality Assurance1234088
February 3, 2023OAIHuman Drugs · Drug Quality Assurance1196557
November 9, 2017VAIHuman Drugs · New Drug Evaluation1031466
May 21, 2015NAIHuman Drugs · Drug Quality Assurance940349
December 17, 2012VAIHuman Drugs · Drug Quality Assurance814448
January 25, 2011NAIHuman Drugs · Drug Quality Assurance709700
September 22, 2009VAIHuman Drugs · Drug Quality Assurance614758
FDA documents

Form 483s (3)

  • Form 483s · March 21, 2024
  • Form 483s · March 11, 2024
  • Form 483s · February 3, 2023
People (5)
Logan T. Williams
Person
Rafeeq A. Habeeb
Person
Travis V. Hull
Person
Robert J. Ham
Person
Rajinder P. Mathura
Person
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Glenmark Pharmaceuticals Ltd
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KVK Tech, Inc.
United Therapeutics Corporation
Societal CDMO Gainesville, LLC
AbbVie Ltd
Company Information

Name

KP Pharmaceutical Technology

FEI Number

3001802820

Address

1212 W Rappel Ave, Bloomington, Indiana 47404, United States

Country

United States

ID: acd7d203-2bd2-4702-a902-83c45f57890f

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