Freudenberg Medical, LLC

Form 483

Carpinteria, California, United StatesFEI 2025182Issued March 27, 2012

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 2025182.

Observations3

Issue DateMarch 27, 2012

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Freudenberg Medical, LLC
Location: Carpinteria, California, United States
FEI Number: 2025182
Product Type: Devices
Issue Date: March 27, 2012
Country: United States

Inspection History, 2009 to 2016

NAI1

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.

Freudenberg Medical, LLC FDA Form 483, Carpinteria, California, March 27, 2012