FDA inspection

Brainlab AG: FDA inspection ending Apr 28, 2005

FDA inspection 383388 · Voluntary Action Indicated (VAI) · Munich

Key facts

Inspection ID 383388
Firm Brainlab AG
FEI number 3002619595
Address Olof-palme-str. 9
City Munich
Fiscal year 2005
Inspection end date Apr 28, 2005
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med 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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