Karl Storz SE & Co. KG

Form 483

Tuttlingen, -, GermanyFEI 3002808268Issued October 18, 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 3002808268.

Observations5

Issue DateOctober 18, 2012

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Karl Storz SE & Co. KG
Location: Tuttlingen, -, Germany
FEI Number: 3002808268
Product Type: Devices
Issue Date: October 18, 2012
Country: Germany

Inspection History, 2010 to 2022

VAI3

OAI1

VAI means Voluntary Action Indicated. OAI means Official 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.

Karl Storz SE & Co. KG FDA Form 483, Tuttlingen, October 18, 2012