FDA Inspection
Lai Chow Kok, MDLai Chow Kok, MD – FDA Inspection, Jun 10, 2013
Record Details
This FDA Inspection record concerns Lai Chow Kok, MD, with an inspection on June 10, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Lai Chow Kok, MD
- Inspection Date
- June 10, 2013
- Product Type
- Devices
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ID · 8fe26aaa-6fed-4fa0-a1f5-bf936bd4770e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 834487
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.140(a)(3)(ii)Investigator adverse effect records inadequate
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