FDA inspection

Cognifit: FDA inspection ending Aug 19, 2025

FDA inspection 1281637 · No Action Indicated (NAI) · San Francisco, CA

Key facts

Inspection ID 1281637
Firm Cognifit
FEI number 3017544020
Address 600 California St Fl 11
City San Francisco
State CA
ZIP 94108-2727
Fiscal year 2025
Inspection end date Aug 19, 2025
Classification No Action Indicated (NAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes 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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