FDA inspection

Mederi Therapeutics, Inc: FDA inspection ending Aug 19, 2015

FDA inspection 939661 · No Action Indicated (NAI) · Norwalk, CT

Key facts

Inspection ID 939661
Firm Mederi Therapeutics, Inc
FEI number 3007729452
Address 800 Connecticut Ave Ste 1E01
City Norwalk
State CT
ZIP 06854
Country United States
Fiscal year 2015
Inspection end date Aug 19, 2015
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

Browse all FDA inspections