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FDA Inspection
•Catalent Belgium SA•November 25, 2016

Catalent Belgium SA – FDA Inspection, Nov 25, 2016

Record Details

This FDA Inspection record concerns Catalent Belgium SA, with an inspection on November 25, 2016, issued by the Center for Veterinary Medicine, covering veterinary.

Company
Catalent Belgium SA
Inspection Date
November 25, 2016
Product Type
Veterinary
Office
Center for Veterinary Medicine
People
  • Ademola O. Daramola
  • Susanne M. Richardson (Company Rep)
View Company Profile

ID · e68d342f-28b8-48c3-81ff-9c0e1951ee63

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
996402
FDA center
Animal Drugs & Feeds
Project area
Pre-Approval Eval. of Animal Drugs and Food Additives
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 211.113(b)Procedures for sterile drug products
  2. 21 CFR 211.42(c)(10)(v)Cleaning System

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Catalent Belgium SA

13
DateClassificationOfficeProject area
July 12, 2024Not classifiedOffice of Inspections and Investigations
April 7, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 19, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 22, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 19, 2019VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
View all 13 other inspections on the company page
Other documents for Catalent Belgium SA
  • FDA Inspection 1273463 - 2024-07-12
  • FDA Inspection 1246550 - 2023-04-07
  • FDA Inspection 1177876 - 2022-08-19
  • FDA Inspection 1136201 - 2020-01-22
  • FDA Inspection 1093395 - 2019-06-19

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