# FDA Inspection 938006 - ActiGraph, LLC - July 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/actigraph-llc/05dafa7b-c05a-4f46-914a-c2297b055673
Source feed: FDA_Inspections

> FDA inspection 938006 of ActiGraph, LLC, July 30, 2015. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 938006
- Company Name: ActiGraph, LLC
- Inspection Date: 2015-07-30
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 985157 - 2016-09-01
- [FDA Inspection 662098 - 2010-05-11](https://www.keypedia.com/records/fda_inspections/actigraph-llc/d0cc704b-524c-42d9-91a6-0f258f33e255)

Company: https://www.keypedia.com/companies/actigraph-llc/027aa9e0-5f9e-4439-8c83-fdbaebbbe2ae

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7