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Catalent Greenville, Inc. — FDA Facility Profile

FEI 3000209735

Catalent Greenville, Inc. is an FDA-registered facility (FEI 3000209735) located in Greenville, NC, US. Registered operations: ANALYSIS; LABEL; MANUFACTURE; PACK. RegDataLab tracks 10 or more FDA inspections at this facility.

Facility Details

Location
Greenville, NC (US)
Registration Expires
December 31, 2026
Operations
ANALYSIS; LABEL; MANUFACTURE; PACK
Source
decrs

Recent inspections

  • 1267356 (VAI Fri Oct 24 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1231042 (NAI Wed Jan 31 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1097051 (VAI Fri Jul 12 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1065149 (NAI Fri Aug 24 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1019260 (NAI Thu Apr 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 983236 (NAI Thu Jul 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 880075 (NAI Fri May 02 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 845560 (NAI Wed Aug 21 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 781692 (VAI Fri May 11 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 781526 (VAI Fri May 11 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Import refusals

  • 799-9729136-3/11/1 (Mon Jul 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources