Eisai, Inc.

Form 483

Baltimore, Maryland, United StatesFEI 1000158705Issued December 17, 2013

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 1000158705.

Observations4

Issue DateDecember 17, 2013

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Eisai, Inc.
Location: Baltimore, Maryland, United States
FEI Number: 1000158705
Product Type: Drugs
Issue Date: December 17, 2013
Country: United States

Inspection History, 2010 to 2024

NAI2

VAI3

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.

Eisai, Inc. FDA Form 483, Baltimore, Maryland, December 17, 2013