FDA Inspection 1203961 — Neurotris, Inc.

Neurotris, Inc. — FEI 3008069988

The FDA completed an inspection of Neurotris, Inc. on April 25, 2023 in Irvine, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
April 25, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures