FDA inspection

Richard Wolf GmbH: FDA inspection ending Oct 20, 2022

FDA inspection 1198730 · Official Action Indicated (OAI) · Knittlingen

Key facts

Inspection ID 1198730
Firm Richard Wolf GmbH
FEI number 3002808001
Address Pforzheimer Str. 32
City Knittlingen
Country Germany
Fiscal year 2023
Inspection end date Oct 20, 2022
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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