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FDA Inspection
•Patheon Manufacturing Services LLC•August 30, 2024

Patheon Manufacturing Services LLC – FDA Inspection, Aug 30, 2024

Record Details

This FDA Inspection record concerns Patheon Manufacturing Services LLC, with an inspection on August 30, 2024, issued by the New Jersey District Office, covering human drugs.

Company
Patheon Manufacturing Services LLC
Inspection Date
August 30, 2024
Product Type
Human Drugs
Office
New Jersey District Office
People
  • Ekaterina Allen (Investigator)
  • Zhong Li
View Company Profile

ID · f9a54ee5-2339-4c55-8d82-45ea527b780e

Inspection Facts

Inspection number
1271322
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Patheon Manufacturing Services LLC

12
DateClassificationOfficeProject area
May 19, 2026Not classifiedNew Jersey District OfficeVaccines and Allergenic Products
June 13, 2024VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
March 18, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 17, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
December 7, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 12 other inspections on the company page
Other documents for Patheon Manufacturing Services LLC
  • FDA Inspection 1317726 - 2026-05-19
  • FDA Inspection 1230469 - 2024-06-13
  • FDA Inspection 1230688 - 2024-03-18
  • FDA Inspection 1076243 - 2018-12-17
  • FDA Inspection 1039401 - 2017-12-07

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