# FDA Inspection 743924 - Towic Medical Inc. - September 09, 2011

Source: https://www.keypedia.com/records/fda_inspections/towic-medical-inc/73c1bdbe-406c-42a3-bd7e-67e1ea0eb930
Source feed: FDA_Inspections

> FDA Inspection 743924 for Towic Medical Inc. on September 09, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 743924
- Company Name: Towic Medical Inc.
- Inspection Date: 2011-09-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 872901 - 2014-04-03](https://www.keypedia.com/records/fda_inspections/towic-medical-inc/7ce9dd60-d9c7-478f-9fc0-7cd627ddd795)
- [FDA Inspection 872901 - 2014-04-03](https://www.keypedia.com/records/fda_inspections/towic-medical-inc/8b86747f-d332-4d34-a60a-3ebd7de6881b)
- [FDA Inspection 743924 - 2011-09-09](https://www.keypedia.com/records/fda_inspections/towic-medical-inc/0a084f74-ac01-437a-8d6c-eb32768ca526)

Company: https://www.keypedia.com/companies/towic-medical-inc/74835070-2db8-4998-81dc-547b92939f6e

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