# FDA Inspection 791042 - Kem Medical Products Corp - July 10, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/kem-medical-products-corp/277950a4-0bbf-43a6-ba7e-5bf968e5832c
Source feed: FDA_Inspections

> FDA Inspection 791042 for Kem Medical Products Corp on July 10, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791042
- Company Name: Kem Medical Products Corp
- Inspection Date: 2012-07-10
- 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.globalkeysolutions.net/companies/kem-medical-products-corp/839eba3c-ce65-4e39-a7a5-7258eddea42a

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