FDA inspection

AMO Uppsala AB: FDA inspection ending Apr 5, 2017

FDA inspection 1011328 · No Action Indicated (NAI) · Uppsala

Key facts

Inspection ID 1011328
Firm AMO Uppsala AB
FEI number 3004750704
Address Rapsgatan 7
City Uppsala
Country Sweden
Fiscal year 2017
Inspection end date Apr 5, 2017
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
  • 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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