JMA Partners – FDA 483 Response, Oct 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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483 RESPONSE

JMA PartnersOctober 21, 2016

JMA Partners – FDA 483 Response, Oct 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)

View Company Profile

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)

Full citation text and observation details available on the Dashboard.

One record shows the event. A profile shows the pattern.

Buy this document for the source file and details behind this single event.

Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.

Explore JMA Partners