FDA Inspection
Catalent Greenville IncCatalent Greenville Inc – FDA Inspection, Nov 13, 2009
Record Details
This FDA Inspection record concerns Catalent Greenville Inc, with an inspection on November 13, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Catalent Greenville Inc
- Inspection Date
- November 13, 2009
- Product Type
- Drugs
View Company Profile
ID · 7e5bdeaf-b9d2-4f96-963b-efa3f0422608
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 631886
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Catalent Greenville Inc
12| Date | Classification | Office | Project area |
|---|---|---|---|
| October 24, 2025 | VAI | Atlanta District Office | Drug Quality Assurance |
| January 31, 2024 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 12, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 24, 2018 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| April 13, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Catalent Greenville Inc
- FDA Inspection 1267356 - 2025-10-24
- FDA Inspection 1231042 - 2024-01-31
- FDA Inspection 1097051 - 2019-07-12
- FDA Inspection 1065149 - 2018-08-24
- FDA Inspection 1019260 - 2017-04-13
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