FDA inspection

INNOVIEW GMBH: FDA inspection ending Jan 28, 2009

FDA inspection 567235 · No Action Indicated (NAI) · Eichstetten

Key facts

Inspection ID 567235
Firm INNOVIEW GMBH
FEI number 3003922255
Address Bruckmatten 35
City Eichstetten
Country Germany
Fiscal year 2009
Inspection end date Jan 28, 2009
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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