# FDA Inspection 998465 - B. Braun Aesculap Japan Co., Ltd. - December 01, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/b-braun-aesculap-japan-co-ltd/12b69b3b-2b21-4367-a0d0-bac697be29fc
Source feed: FDA_Inspections

> FDA Inspection 998465 for B. Braun Aesculap Japan Co., Ltd. on December 01, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 998465
- Company Name: B. Braun Aesculap Japan Co., Ltd.
- Inspection Date: 2016-12-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 877308 - 2014-04-10](https://www.globalkeysolutions.net/records/fda_inspections/b-braun-aesculap-japan-co-ltd/641ce802-eeeb-46c4-82b7-7e5333909faa)

Company: https://www.globalkeysolutions.net/companies/b-braun-aesculap-japan-co-ltd/2b68ba53-9b6c-4755-8514-c876a2b766f7

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7