FDA inspection
Bayer AG: FDA inspection ending May 27, 2010
FDA inspection 667944 · Administrative/Directed Change (ADC) · Berlin
Key facts
| Inspection ID | 667944 |
|---|---|
| Firm | Bayer AG |
| FEI number | 3002808086 |
| Address | Mullerstr. 170-178 |
| City | Berlin |
| Fiscal year | 2010 |
| Inspection end date | May 27, 2010 |
| Classification | Administrative/Directed Change (ADC) |
| Project area | Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human Drugs|Post Mrkt Surv & Epid: Human 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Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs|Postmarketing Surveillance and Epidemiology: Human Drugs |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data