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FDA Inspection
•Catalent Indiana, LLC•December 15, 2011

Catalent Indiana, LLC – FDA Inspection, Dec 15, 2011

Record Details

This FDA Inspection record concerns Catalent Indiana, LLC, with an inspection on December 15, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company
Catalent Indiana, LLC
Inspection Date
December 15, 2011
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 7cd1c84e-8c16-4c8d-bfe0-c91e94515b67

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
759064
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

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
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Brooklyn, NY 11201
Scranton Office:
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Scranton, PA, 18503
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