# FDA Inspection 805920 - Hontech Foundation, LLC - October 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/hontech-foundation-llc/1d3436bc-5a76-4940-834d-e151ebe3e149
Source feed: FDA_Inspections

> FDA Inspection 805920 for Hontech Foundation, LLC on October 23, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 805920
- Company Name: Hontech Foundation, LLC
- Inspection Date: 2012-10-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 571634 - 2009-03-25](https://www.keypedia.com/records/fda_inspections/hontech-foundation-llc/223d1bcc-d3c8-4fb4-9af2-f2605a760c3c)
- [FDA Inspection 571634 - 2009-03-25](https://www.keypedia.com/records/fda_inspections/hontech-foundation-llc/d51b4d1b-effa-4b89-978c-f06851bcc3e3)

Company: https://www.keypedia.com/companies/hontech-foundation-llc/d7440f76-0901-4b28-bd5f-d420421c71b9

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