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FDA Inspection
•Catalent Indiana, LLC•May 1, 2018

Catalent Indiana, LLC – FDA Inspection, May 1, 2018

Record Details

This FDA Inspection record concerns Catalent Indiana, LLC, with an inspection on May 1, 2018, issued by the Detroit District Office, covering human drugs.

Company
Catalent Indiana, LLC
Inspection Date
May 1, 2018
Product Type
Human Drugs
Office
Detroit District Office
People
  • Nicholas L. Paulin (FDA Associated Person)
  • Scott R. Nichols (Issuing Officer)
View Company Profile

ID · d8e8f311-21ec-414b-8603-89ad42244ae3

Inspection Facts

Inspection number
1053499
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Catalent Indiana, LLC

15
DateClassificationOfficeProject area
April 24, 2026Not classifiedDetroit District Office
July 14, 2025OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 15, 2023VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
May 12, 2023Not classifiedDetroit District Office
September 1, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 15 other inspections on the company page
Other documents for Catalent Indiana, LLC
  • FDA Inspection 1317904 - 2026-04-24
  • FDA Inspection 1264264 - 2025-07-14
  • FDA Inspection 1224264 - 2023-11-15
  • FDA Inspection 1208718 - 2023-05-12
  • FDA Inspection 1178819 - 2022-09-01

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
🇺🇸+1 917-789-5099
🇪🇺+48 532-447-507
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