# FDA Inspection 916725 - Kunshan Radiant Innovation Co., Ltd - January 27, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/kunshan-radiant-innovation-co-ltd/883aa343-39bc-4438-8126-05681ab48834
Source feed: FDA_Inspections

> FDA Inspection 916725 for Kunshan Radiant Innovation Co., Ltd on January 27, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 916725
- Company Name: Kunshan Radiant Innovation Co., Ltd
- Inspection Date: 2015-01-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 828893 - 2013-03-29](https://www.globalkeysolutions.net/records/fda_inspections/kunshan-radiant-innovation-co-ltd/f88b2e2c-8c1c-4553-8ceb-46d6cf993a97)

Company: https://www.globalkeysolutions.net/companies/kunshan-radiant-innovation-co-ltd/cd58d39d-d366-4958-a125-dd09df53dbdc

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