FDA Inspection
Catalent Belgium SACatalent Belgium SA – FDA Inspection, Jul 31, 2018
Record Details
This FDA Inspection record concerns Catalent Belgium SA, with an inspection on July 31, 2018, issued by the Center for Devices and Radiological Health, covering devices.
- People
- James W. Whitney (Issuing Officer)
- Lisa B. Orr (Issuing Officer)
- Youmin Wang (Company Rep)
View Company Profile
ID · 7d7ec872-9d8f-4a15-82c9-a72e04b548cf
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1061068
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Catalent Belgium SA
13| Date | Classification | Office | Project area |
|---|---|---|---|
| July 12, 2024 | Not classified | Office of Inspections and Investigations | |
| April 7, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 19, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 22, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 19, 2019 | VAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
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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