# L&K Biomed Co., Ltd. – FDA Inspection, Jan 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/lk-biomed-co-ltd/7738d721-9139-4f11-bb1d-ee8436274cd4
Source feed: FDA_Inspections

> FDA inspection 1000624 of L&K Biomed Co., Ltd., January 26, 2017. Classification: Official Action Indicated (OAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000624
- Company Name: L&K Biomed Co., Ltd.
- Inspection Date: 2017-01-26
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 885364 - 2014-06-05

## Related Officers

- [Investigator](https://www.keypedia.com/people/ashley-a-mutawakkil/512be391-fd96-451c-9569-98e43cfba9db)

Company: https://www.keypedia.com/companies/lk-biomed-co-ltd/251c0cb1-8ca7-4f9e-aac7-45874b6e1de7

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