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FDA Inspection
•Catalent Pharma Solutions, LLC•January 25, 2024

Catalent Pharma Solutions, LLC – FDA Inspection, Jan 25, 2024

Record Details

This FDA Inspection record concerns Catalent Pharma Solutions, LLC, with an inspection on January 25, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company
Catalent Pharma Solutions, LLC
Inspection Date
January 25, 2024
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Monica C. Burgos Garcia
View Company Profile

ID · 89878bd4-947c-4510-8ccf-a1be0821f108

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1229344
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Catalent Pharma Solutions, LLC

11
DateClassificationOfficeProject area
January 30, 2026Not classifiedFlorida District Office
May 30, 2024NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 21, 2023VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
August 28, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
February 22, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 11 other inspections on the company page
Other documents for Catalent Pharma Solutions, LLC
  • FDA Inspection 1282788 - 2026-01-30
  • FDA Inspection 1229815 - 2024-05-30
  • FDA Inspection 1210540 - 2023-07-21
  • FDA Inspection 1101180 - 2019-08-28
  • FDA Inspection 1080109 - 2019-02-22

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