FDA 483_RESPONSE - JMA Partners - October 21, 2016

Record Details

This 483 RESPONSE record concerns JMA Partners, with an inspection on October 21, 2016, issued by the Office of Health Technology 5 (Neurological and Physical Medicine Devices), covering devices.

Company: JMA Partners
Inspection Date: October 21, 2016
Product Type: Devices
Office: Office of Health Technology 5 (Neurological and Physical Medicine Devices)
People: Jack R. Munn
Reynaldo Rodriguez (District Director)

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ID · 3c0ff8aa-b814-4b9d-844f-682d71d2d759

Violation Codes5

21 U.S.C. 33121 CFR 21021 CFR 310.305FD&C Act 501(a)(2)(B)FD&C Act 801(a)(3)

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