# FDA Inspection 944070 - Lin-Zhi International Inc - September 03, 2015

Source: https://www.keypedia.com/records/fda_inspections/lin-zhi-international-inc/d3f04265-5efc-4c77-9b6c-94f1609d3d45
Source feed: FDA_Inspections

> FDA Inspection 944070 for Lin-Zhi International Inc on September 03, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 944070
- Company Name: Lin-Zhi International Inc
- Inspection Date: 2015-09-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 782332 - 2012-05-15](https://www.keypedia.com/records/fda_inspections/lin-zhi-international-inc/9ea91093-5408-47b7-99eb-33ae71f01d6e)
- [FDA Inspection 782332 - 2012-05-15](https://www.keypedia.com/records/fda_inspections/lin-zhi-international-inc/8776d28c-e480-4de7-aa6b-c48165a0416e)
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- [FDA Inspection 698572 - 2010-11-22](https://www.keypedia.com/records/fda_inspections/lin-zhi-international-inc/d13ceacc-57ca-44cd-989d-baf14b43139e)

Company: https://www.keypedia.com/companies/lin-zhi-international-inc/5633e32d-7a88-4899-b5b9-cd6a8e225373

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