FDA inspection

Technolas Perfect Vision GmbH: FDA inspection ending Apr 3, 2008

FDA inspection 516500 · No Action Indicated (NAI) · Munich

Key facts

Inspection ID 516500
Firm Technolas Perfect Vision GmbH
FEI number 3003691824
Address Messerschmittstrasse 1 + 3
City Munich
Fiscal year 2008
Inspection end date Apr 3, 2008
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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

Browse all FDA inspections