FDA Inspection
Upjohn Manufacturing Ireland Unlimited CompanyUpjohn Manufacturing Ireland Unlimited Company – FDA Inspection, Nov 25, 2016
Record Details
This FDA Inspection record concerns Upjohn Manufacturing Ireland Unlimited Company, with an inspection on November 25, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- November 25, 2016
- Product Type
- Drugs
View Company Profile
ID · f155cfef-8390-4790-8d83-c342ee652494
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 994065
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Upjohn Manufacturing Ireland Unlimited Company
5| Date | Classification | Office | Project area |
|---|---|---|---|
| January 26, 2024 | Not classified | Office of Inspections and Investigations | |
| July 2, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 31, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 11, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 17, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Upjohn Manufacturing Ireland Unlimited Company
- FDA Inspection 1316126 - 2024-01-26
- FDA Inspection 1156269 - 2021-07-02
- FDA Inspection 1107158 - 2018-08-31
- FDA Inspection 886485 - 2014-04-11
- FDA Inspection 733195 - 2011-06-17
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