Catalent Belgium SA

Form 483FOIA Uncovered

Brussels, -FEI 3007647000Issued July 31, 2018

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3007647000.

ObservationsNot available

Issue DateJuly 31, 2018

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Catalent Belgium SA
Location: Brussels, -
FEI Number: 3007647000
Product Type: Biologics
Issue Date: July 31, 2018
Country: United States

Inspection History, 2013 to 2023

NAI1

VAI9

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Catalent Belgium SA FDA Form 483, Brussels, July 31, 2018