FDA Inspection
ActiGraph, LLCFDA Inspection 938006 - ActiGraph, LLC - July 30, 2015
Record Details
This FDA Inspection record concerns ActiGraph, LLC, with an inspection on July 30, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- ActiGraph, LLC
- Inspection Date
- July 30, 2015
- Product Type
- Devices
View Company Profile
ID · b9f608c0-5edf-4d81-8d01-997dd6bd8106
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 938006
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of ActiGraph, LLC
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 1, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 11, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for ActiGraph, LLC
- FDA Inspection 985157 - 2016-09-01
- FDA Inspection 662098 - 2010-05-11
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