FDA Center for Devices & Radiological Health Issues Warning Letter to Physitemp Instruments
April 01, 2026
April 01, 2026
WASHINGTON, April 1 -- The U.S. Department of Health and Human Services Food and Drug Administration issued the following warning letter to Physitemp Instruments LLC from its Center for Devices and Radiological Health:
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Recipient: Michele J. Cantwell, Vice President of Sales and Marketing, Physitemp Instruments, LLC, 189 Sargeant Avenue, Clifton, NJ 07013, United States, (b)(4)
Issuing Office: Center for Devices and Radiological Health, United States
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Recipient: Michele J. Cantwell, Vice President of Sales and Marketing, Physitemp Instruments, LLC, 189 Sargeant Avenue, Clifton, NJ 07013, United States, (b)(4)
Issuing Office: Center for Devices and Radiological Health, United States
