FDA inspection

Corden Pharma Chenove: FDA inspection ending Aug 26, 2016

FDA inspection 988106 · No Action Indicated (NAI) · Chenove

Key facts

Inspection ID 988106
Firm Corden Pharma Chenove
FEI number 3002808295
Address Synkem, Corden Pharma Chenove; 47 Rue De Longvic; Bp 50
City Chenove
Country France
Fiscal year 2016
Inspection end date Aug 26, 2016
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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