FDA inspection
B. Braun Aesculap Japan Co., Ltd.: FDA inspection ending Dec 1, 2016
FDA inspection 998465 · Voluntary Action Indicated (VAI) · Tochigitochigi
Key facts
| Inspection ID | 998465 |
|---|---|
| Firm | B. Braun Aesculap Japan Co., Ltd. |
| FEI number | 3005732259 |
| Address | Tochigi Plant, 285 Ogakitsuga-Machi, |
| City | Tochigitochigi |
| Country | Japan |
| Fiscal year | 2017 |
| Inspection end date | Dec 1, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 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