FDA Inspection 1027756 — Neurodynamics, Inc.

Neurodynamics, Inc. — FEI 2434444

The FDA completed an inspection of Neurodynamics, Inc. on October 4, 2017 in New York, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 4, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
New York, NY (United States)

Citations

IDCFRDescription
237121 CFR 820.30(a)Design control - no procedures