# FDA 483 - BK Meditech Co., Ltd. - January 10, 2020

Source: https://www.globalkeysolutions.net/records/483/bk-meditech-co-ltd/175f56e6-9079-4684-b4df-a891b0f118e3

> FDA 483 for BK Meditech Co., Ltd. on January 10, 2020. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: BK Meditech Co., Ltd.
- Inspection Date: 2020-01-10
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)

## Related Documents

- [483 - 2020-01-10](https://www.globalkeysolutions.net/records/483/bk-meditech-co-ltd/7dc687b2-66f6-40e9-8359-d1c69710be2f)

## Related Officers

- [Thai T. Duong](https://www.globalkeysolutions.net/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

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

Office: https://www.globalkeysolutions.net/offices/division-of-clinical-evidence-and-analysis-1-clinical-policy-and-quality/5f95da17-30bb-423f-b892-5ea041823fbd