FDA Inspection
Bayer OYBayer OY – FDA Inspection, Jun 1, 2018
Record Details
This FDA Inspection record concerns Bayer OY, with an inspection on June 1, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · eb270355-f562-4afe-a57d-a5516d1fec89
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1055914
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Bayer OY
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 15, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 15, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 2, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 15, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 24, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Bayer OY
- FDA Inspection 1273226 - 2023-09-15
- FDA Inspection 972548 - 2016-04-15
- FDA Inspection 803182 - 2012-10-02
- FDA Inspection 762223 - 2011-12-15
- FDA Inspection 694779 - 2010-09-24
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