FDA inspection

Delpharm Dijon: FDA inspection ending May 31, 2024

FDA inspection 1240699 · Voluntary Action Indicated (VAI) · Quetigny

Key facts

Inspection ID 1240699
Firm Delpharm Dijon
FEI number 3014120699
Address 6 Boulevard De L Europe
City Quetigny
Fiscal year 2024
Inspection end date May 31, 2024
Classification Voluntary Action Indicated (VAI)
Project area Generic Drug Evaluation
Product type Drugs

At a glance

  • 1–9 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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