FDA inspection

OPTILASA, S.L.: FDA inspection ending Jun 2, 2010

FDA inspection 669185 · Official Action Indicated (OAI) · Madrid

Key facts

Inspection ID 669185
Firm OPTILASA, S.L.
FEI number 3001022138
Address Calle De Arturo Soria 338
City Madrid
Country Spain
Fiscal year 2010
Inspection end date Jun 2, 2010
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 10–99 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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