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FDA Inspection
•Catalent Pharma Solutions, LLC•January 30, 2026

Catalent Pharma Solutions, LLC – FDA Inspection, Jan 30, 2026

Record Details

This FDA Inspection record concerns Catalent Pharma Solutions, LLC, with an inspection on January 30, 2026, issued by the Florida District Office, covering human drugs.

Company
Catalent Pharma Solutions, LLC
Inspection Date
January 30, 2026
Product Type
Human Drugs
Office
Florida District Office
People
  • Damaris Y. Hernandez (Investigator)
  • Danny T. Fernandez (Issuing Officer)
  • Denny Y. Fernandez (Issuing Officer)
  • Nicole E. Knowlton (FDA Associated Person)
  • Tammy T. Brown (Company Rep)
View Company Profile

ID · 3c033b5d-6772-4e48-87f5-c003b37a8034

Inspection Facts

Inspection number
1282788
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Catalent Pharma Solutions, LLC

11
DateClassificationOfficeProject area
May 30, 2024NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 25, 2024NAICenter for Devices and Radiological HealthCompliance: Devices
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 1229815 - 2024-05-30
  • FDA Inspection 1229344 - 2024-01-25
  • FDA Inspection 1210540 - 2023-07-21
  • FDA Inspection 1101180 - 2019-08-28
  • FDA Inspection 1080109 - 2019-02-22

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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
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🇪🇺+48 532-447-507
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