FDA inspection

Integrum Ab: FDA inspection ending Sep 8, 2022

FDA inspection 1180268 · Voluntary Action Indicated (VAI) · Molndal

Key facts

Inspection ID 1180268
Firm Integrum Ab
FEI number 3011386779
Address Krokslatts Fabriker 50
City Molndal
Country Sweden
Fiscal year 2022
Inspection end date Sep 8, 2022
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
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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