FDA inspection

Merz North America, Inc.: FDA inspection ending May 25, 2010

FDA inspection 663790 · No Action Indicated (NAI) · Raleigh, NC

Key facts

Inspection ID 663790
Firm Merz North America, Inc.
FEI number 1012187
Address 1840 S Stapley Dr Ste 200
City Raleigh
State NC
ZIP 27615
Country United States
Fiscal year 2010
Inspection end date May 25, 2010
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
  • 10–99 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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