# FDA Inspection 890849 - KAIWEI SHENZHEN CO., LTD - July 17, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/kaiwei-shenzhen-co-ltd/b9515850-540b-4492-9849-91128db36990
Source feed: FDA_Inspections

> FDA Inspection 890849 for KAIWEI SHENZHEN CO., LTD on July 17, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 890849
- Company Name: KAIWEI SHENZHEN CO., LTD
- Inspection Date: 2014-07-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 890849 - 2014-07-17](https://www.globalkeysolutions.net/records/fda_inspections/kaiwei-shenzhen-co-ltd/deac460e-5196-4167-af5b-f0245b9b4869)

Company: https://www.globalkeysolutions.net/companies/kaiwei-shenzhen-co-ltd/fac92697-d4fb-4b23-befc-1fe06b79ce91

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