by ComplianceQuest

Inspection Tracker

Tracker Overview Enforcement Themes Form 483s Warning Letters Inspections Recalls Investigators Companies Facilities

FDA Guidance Global Templates

Start with a Free ConsultationBook 30 minutes with a ComplianceQuest specialist.Book a Call

Sign In Create a Free Account

Big News: FDA is moving from MasterControl to ComplianceQuest.See Why

Search AgentQ/

Talk to a Specialist

Loading…

My DashboardInspection TrackerForm 483sCelltrion Inc.

Celltrion Inc.

Form 483FOIA Uncovered

Korea (the Republic Of)Issued February 16, 2018

View FDA's Record for This Firm

Source: FDA record for this establishment. FDA publishes inspections or enforcement actions for this establishment, listed further down this page, but we have not matched this particular Form 483 to a document or an inspection date FDA has released. It stays out of the default view for that reason.

ObservationsNot available

Issue DateFebruary 16, 2018

StatusWarning Letter Issued

Related Inspections0

Establishment Details

Firm: Celltrion Inc.
Location: Korea (the Republic Of)
FEI Number: N/A
Issue Date: February 16, 2018
Country: Korea (the Republic Of)

Inspection History

We hold no FDA inspection matched to this establishment.

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.

Celltrion Inc. FDA Form 483, February 16, 2018