# FDA Inspection 808939 - Rehm Kenneth, DMP - November 30, 2012

Source: https://www.keypedia.com/records/fda_inspections/rehm-kenneth-dmp/8dfcb297-fd28-483c-b309-94b5e07c7750
Source feed: FDA_Inspections

> FDA Inspection 808939 for Rehm Kenneth, DMP on November 30, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 808939
- Company Name: Rehm Kenneth, DMP
- Inspection Date: 2012-11-30
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/rehm-kenneth-dmp/2e0278db-9642-4c6a-bb71-a5d12114a8b6

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