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FDA Inspection
•Motive Health, Inc.•October 17, 2017

Motive Health, Inc. – FDA Inspection, Oct 17, 2017

Record Details

This FDA Inspection record concerns Motive Health, Inc., with an inspection on October 17, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Motive Health, Inc.
Inspection Date
October 17, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Charles L. Larson (Company Rep)
View Company Profile

ID · 30f0a1bf-4a7b-417d-8cbb-5e524758da88

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1028993
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 820.198(e)Records of complaint investigation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Motive Health, Inc.

2
DateClassificationOfficeProject area
November 3, 2023NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 22, 2021NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Motive Health, Inc.
  • FDA Inspection 1223220 - 2023-11-03
  • FDA Inspection 1159756 - 2021-11-22

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