# FDA Inspection 623870 - Kem Medical Products Corp - October 27, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/kem-medical-products-corp/165ba505-13bc-4afa-9939-823eec7a350b
Source feed: FDA_Inspections

> FDA Inspection 623870 for Kem Medical Products Corp on October 27, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 623870
- Company Name: Kem Medical Products Corp
- Inspection Date: 2009-10-27
- Classification: Voluntary Action Indicated (VAI)
- 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