# FDA Inspection 763521 - Smartech Precision Ceramic Rech. (Shenzhen) Co., Ltd. - December 22, 2011

Source: https://www.keypedia.com/records/fda_inspections/smartech-precision-ceramic-rech-shenzhen-co-ltd/0ad46433-f994-4fb4-ac8a-6d92a67bdac7
Source feed: FDA_Inspections

> FDA Inspection 763521 for Smartech Precision Ceramic Rech. (Shenzhen) Co., Ltd. on December 22, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 763521
- Company Name: Smartech Precision Ceramic Rech. (Shenzhen) Co., Ltd.
- Inspection Date: 2011-12-22
- 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/smartech-precision-ceramic-rech-shenzhen-co-ltd/bb22d08d-9bc6-46f3-bfa7-e6c5a36b6a93

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