Richard Wolf GmbH

Form 483

Knittlingen, -, GermanyFEI 3002808001Issued June 10, 2010

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 3002808001.

Observations1

Issue DateJune 10, 2010

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Richard Wolf GmbH
Location: Knittlingen, -, Germany
FEI Number: 3002808001
Product Type: Devices
Issue Date: June 10, 2010
Country: Germany

Inspection History, 2010 to 2022

NAI1

VAI2

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Richard Wolf GmbH FDA Form 483, Knittlingen, June 10, 2010