# ActiGraph, LLC - Inspection Records

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

> Inspection records and compliance data for ActiGraph, LLC in Pensacola, Florida. Access full analysis and detailed observations.

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## Details

- Name: ActiGraph, LLC
- FEI Number: 3006254866
- City: Pensacola
- State: Florida
- Country Name: United States
- Address Line 1: 70 N Baylen St Ste 400
- Zip Code: 32502

## Related Documents

- [FDA Inspection 985157 - ActiGraph, LLC - 2016-09-01](https://www.keypedia.com/records/fda_inspections/actigraph-llc/a1708921-9f63-4909-990e-1610c63b334b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 1, 2016
- [FDA Inspection 985157 - ActiGraph, LLC - 2016-09-01](https://www.keypedia.com/records/fda_inspections/actigraph-llc/5700402d-43fe-4b27-9f15-3034ee174e55) — classification: No Action Indicated (NAI), source: FDA, date: September 1, 2016
- [483 - ActiGraph, LLC - 2015-07-30](https://www.keypedia.com/records/483/actigraph-llc/15e9a66a-89b3-4a2b-a6c3-99beadabba65) — source: FDA, date: July 30, 2015
- [FDA Inspection 938006 - ActiGraph, LLC - 2015-07-30](https://www.keypedia.com/records/fda_inspections/actigraph-llc/b9f608c0-5edf-4d81-8d01-997dd6bd8106) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 30, 2015
- [FDA Inspection 938006 - ActiGraph, LLC - 2015-07-30](https://www.keypedia.com/records/fda_inspections/actigraph-llc/05dafa7b-c05a-4f46-914a-c2297b055673) — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2015
- [FDA Inspection 662098 - ActiGraph, LLC - 2010-05-11](https://www.keypedia.com/records/fda_inspections/actigraph-llc/d0cc704b-524c-42d9-91a6-0f258f33e255) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 11, 2010
- [FDA Inspection 662098 - ActiGraph, LLC - 2010-05-11](https://www.keypedia.com/records/fda_inspections/actigraph-llc/73371316-39f3-4395-acb3-31bdac5707e9) — classification: No Action Indicated (NAI), source: FDA, date: May 11, 2010

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