# FDA Inspection 1000624 - L&K Biomed Co., Ltd. - January 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/lk-biomed-co-ltd/5f4faeb9-90bd-4080-a516-8b7c866afa54
Source feed: FDA_Inspections

> FDA Inspection 1000624 for L&K Biomed Co., Ltd. on January 26, 2017. Classification: Official Action Indicated (OAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1000624 - 2017-01-26](https://www.keypedia.com/records/fda_inspections/lk-biomed-co-ltd/7738d721-9139-4f11-bb1d-ee8436274cd4)
- [FDA Inspection 885364 - 2014-06-05](https://www.keypedia.com/records/fda_inspections/lk-biomed-co-ltd/b8ff5771-1f94-43f3-afec-51c1a9a2dce1)

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