# Kerma Medical Products, Inc – FDA Inspection, Nov 4, 2011

Source: https://www.keypedia.com/records/fda_inspections/kerma-medical-products-inc/7dd03706-42b3-4fee-aa7f-c76afab662a1
Source feed: FDA_Inspections

> FDA inspection 752181 of Kerma Medical Products, Inc, November 04, 2011. Classification: Voluntary Action Indicated (VAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 752181
- Company Name: Kerma Medical Products, Inc
- Inspection Date: 2011-11-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1024609 - 2017-07-07
- [FDA Inspection 863395 - 2014-01-23](https://www.keypedia.com/records/fda_inspections/kerma-medical-products-inc/22972682-7e26-40de-ac5b-15f67e82e8d6)

Company: https://www.keypedia.com/companies/kerma-medical-products-inc/bb96e435-46df-43ce-b968-771b7abe04f3

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