FDA inspection

Curasan AG: FDA inspection ending May 12, 2017

FDA inspection 1015620 · No Action Indicated (NAI) · Kleinostheim

Key facts

Inspection ID 1015620
Firm Curasan AG
FEI number 3003771570
Address Lindigstr. 4
City Kleinostheim
Country Germany
Fiscal year 2017
Inspection end date May 12, 2017
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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