FDA inspection

NeuroOne Medical Technologies Corporation: FDA inspection ending Dec 16, 2021

FDA inspection 1159398 · No Action Indicated (NAI) · Eden Prairie, MN

Key facts

Inspection ID 1159398
Firm NeuroOne Medical Technologies Corporation
FEI number 3016438686
Address 7599 Anagram Dr
City Eden Prairie
State MN
ZIP 55344
Country United States
Fiscal year 2022
Inspection end date Dec 16, 2021
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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