FDA inspection

Circassia AB: FDA inspection ending Sep 11, 2019

FDA inspection 1120602 · Voluntary Action Indicated (VAI) · Uppsala

Key facts

Inspection ID 1120602
Firm Circassia AB
FEI number 3008662397
Address Hansellisgatan 13
City Uppsala
Fiscal year 2019
Inspection end date Sep 11, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None 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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