FDA inspection

Apotek Production & Laboratorier: FDA inspection ending Mar 5, 2015

FDA inspection 922596 · Administrative/Directed Change (ADC) · Umea

Key facts

Inspection ID 922596
Firm Apotek Production & Laboratorier
FEI number 3003766921
Address Formvagen 5B
City Umea
Fiscal year 2015
Inspection end date Mar 5, 2015
Classification Administrative/Directed Change (ADC)
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Product type Devices

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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