# FDA Inspection 858496 - BK Meditech Co., Ltd. - November 21, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/bk-meditech-co-ltd/c088221c-00b4-432e-92ad-18010988de29
Source feed: FDA_Inspections

> FDA Inspection 858496 for BK Meditech Co., Ltd. on November 21, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 858496
- Company Name: BK Meditech Co., Ltd.
- Inspection Date: 2013-11-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 858496 - 2013-11-21](https://www.globalkeysolutions.net/records/fda_inspections/bk-meditech-co-ltd/f50a82e2-bcc7-45cd-b223-fccc1c161bca)
- [FDA Inspection 662531 - 2010-05-06](https://www.globalkeysolutions.net/records/fda_inspections/bk-meditech-co-ltd/b8177c78-ae5f-460b-9acc-c694a7ae3824)

Company: https://www.globalkeysolutions.net/companies/bk-meditech-co-ltd/2f915d05-c058-420a-9dce-516fcfa908c4

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