FDA inspection

Merck Sharp & Dohme BV: FDA inspection ending Nov 20, 2014

FDA inspection 903950 · No Action Indicated (NAI) · Haarlem

Key facts

Inspection ID 903950
Firm Merck Sharp & Dohme BV
FEI number 3002807658
Address Waarderweg 39
City Haarlem
Country Netherlands
Fiscal year 2015
Inspection end date Nov 20, 2014
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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