FDA Inspection
Kai Yi Co.Kai Yi Co. – FDA Inspection, Sep 23, 2014
Record Details
This FDA Inspection record concerns Kai Yi Co., with an inspection on September 23, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kai Yi Co.
- Inspection Date
- September 23, 2014
- Product Type
- Devices
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ID · 80d90847-a176-489b-88cf-def7a63be113
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 900803
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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