Argen Corporation, The

Form 483

San Diego, California, United StatesFEI 2433919Issued December 12, 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 2433919.

Observations5

Issue DateDecember 12, 2013

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Argen Corporation, The
Location: San Diego, California, United States
FEI Number: 2433919
Product Type: Devices
Issue Date: December 12, 2013
Country: United States

Inspection History, 2009 to 2013

NAI1

VAI1

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.

Argen Corporation, The FDA Form 483, San Diego, California, December 12, 2013