# FDA Inspection 752181 - Kerma Medical Products, Inc - November 04, 2011

Source: https://www.keypedia.com/records/fda_inspections/kerma-medical-products-inc/3b3eb470-b648-4631-a3ee-9a18ac5c45c8
Source feed: FDA_Inspections

> FDA Inspection 752181 for Kerma Medical Products, Inc on November 04, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 752181
- Company Name: Kerma Medical Products, Inc
- Inspection Date: 2011-11-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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