FDA Inspection 850702 - STERIMED, Inc. - September 27, 2013

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Record Details

This FDA Inspection record concerns STERIMED, Inc., with an inspection on September 27, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: STERIMED, Inc.
Inspection Date: September 27, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · edc68029-ed69-4637-8a3b-c2933fc07b4d