FDA Inspection
Boehringer Ingelheim Pharma Gmbh & Co KgBoehringer Ingelheim Pharma Gmbh & Co Kg – FDA Inspection, Sep 21, 2018
Record Details
This FDA Inspection record concerns Boehringer Ingelheim Pharma Gmbh & Co Kg, with an inspection on September 21, 2018, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- September 21, 2018
- Product Type
- Human Drugs
- Person
- Diane L. Raccasi (Issuing Officer)
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ID · 03de647a-2e62-474d-97a1-988dcb0acf6b
Inspection Facts
- Inspection number
- 1069908
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Boehringer Ingelheim Pharma Gmbh & Co Kg
13| Date | Classification | Office | Project area |
|---|---|---|---|
| July 22, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 19, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 15, 2019 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| April 5, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 19, 2018 | Not classified | Office of Inspections and Investigations |
Other documents for Boehringer Ingelheim Pharma Gmbh & Co Kg
- FDA Inspection 1208927 - 2022-07-22
- FDA Inspection 1102691 - 2019-09-19
- FDA Inspection 1107587 - 2019-08-15
- FDA Inspection 1086418 - 2019-04-05
- FDA Inspection 1072835 - 2018-10-19
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