FDA inspection

Berlimed, S.A.: FDA inspection ending Sep 25, 2018

FDA inspection 1066603 · Voluntary Action Indicated (VAI) · Alcala de Henares

Key facts

Inspection ID 1066603
Firm Berlimed, S.A.
FEI number 3004492234
Address Poligono Industrial Santa Rosa, Calle Francisco Alonso 7
City Alcala de Henares
Country Spain
Fiscal year 2018
Inspection end date Sep 25, 2018
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 Citations
  • 1–9 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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