FDA inspection

Moeller Medical GmbH: FDA inspection ending Nov 2, 2005

FDA inspection 405761 · No Action Indicated (NAI) · Fulda

Key facts

Inspection ID 405761
Firm Moeller Medical GmbH
FEI number 3002807634
Address Wasserkuppenstr. 29-31
City Fulda
Fiscal year 2006
Inspection end date Nov 2, 2005
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

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