FDA Inspection 985157 — ActiGraph, LLC

ActiGraph, LLC — FEI 3006254866

The FDA completed an inspection of ActiGraph, LLC on Sep 1, 2016 in Pensacola, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 1, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Pensacola, FL (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures

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