# FDA Inspection 939040 - Jianyi Enterprises - July 15, 2015

Source: https://www.keypedia.com/records/fda_inspections/jianyi-enterprises/0aae0be1-a456-4691-9b77-9cfe13d11d86
Source feed: FDA_Inspections

> FDA Inspection 939040 for Jianyi Enterprises on July 15, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 939040
- Company Name: Jianyi Enterprises
- Inspection Date: 2015-07-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 939040 - 2015-07-15](https://www.keypedia.com/records/fda_inspections/jianyi-enterprises/d6d9244a-99e3-4525-9129-a3ae83680f56)

Company: https://www.keypedia.com/companies/jianyi-enterprises/f1c8ac5d-9486-4eaf-b27b-4f9fb5590ea4

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