FDA inspection

Delpharm Dijon: FDA inspection ending Nov 19, 2021

FDA inspection 1229926 · Voluntary Action Indicated (VAI) · Quetigny

Key facts

Inspection ID 1229926
Firm Delpharm Dijon
FEI number 3014120699
Address 6 Boulevard De L Europe
City Quetigny
Country France
Fiscal year 2022
Inspection end date Nov 19, 2021
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 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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