FDA Inspection
L&K Biomed Co., Ltd.L&K Biomed Co., Ltd. – FDA Inspection, Jan 26, 2017
Record Details
This FDA Inspection record concerns L&K Biomed Co., Ltd., with an inspection on January 26, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 7738d721-9139-4f11-bb1d-ee8436274cd4
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 1000624
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of L&K Biomed Co., Ltd.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 5, 2014 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for L&K Biomed Co., Ltd.
- FDA Inspection 885364 - 2014-06-05
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