FDA inspection

Alma Lasers GMBH: FDA inspection ending Jan 24, 2008

FDA inspection 504692 · No Action Indicated (NAI) · Nuremberg

Key facts

Inspection ID 504692
Firm Alma Lasers GMBH
FEI number 3002483854
Address Nordostpark 100-102
City Nuremberg
Fiscal year 2008
Inspection end date Jan 24, 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