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Delpharm DIjon — FDA Facility Profile

FEI 3014120699

Delpharm DIjon is an FDA-registered facility (FEI 3014120699) located in Quetigny, FR. Registered operations: MANUFACTURE; PACK. RegDataLab tracks 1 FDA inspection at this facility.

Facility Details

Location
Quetigny (FR)
Registration Expires
December 31, 2026
Operations
MANUFACTURE; PACK
Source
decrs

Recent inspections

  • 1229926 (VAI Fri Nov 19 2021 00:00:00 GMT+0000 (Coordinated Universal Time))

Import refusals

  • 1FX-3800896-7/10002/1 (Thu Jul 02 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-7888202-1/21/1 (Tue Oct 20 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-6300300-5/11/1 (Tue Sep 10 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources