# FDA Inspection 900803 - Kai Yi Co. - September 23, 2014

Source: https://www.keypedia.com/records/fda_inspections/kai-yi-co/80d90847-a176-489b-88cf-def7a63be113
Source feed: FDA_Inspections

> FDA Inspection 900803 for Kai Yi Co. on September 23, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900803
- Company Name: Kai Yi Co.
- Inspection Date: 2014-09-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/kai-yi-co/83b187f9-48eb-4741-81d8-49a7088b85e9

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