FDA inspection

Directa AB: FDA inspection ending Sep 5, 2019

FDA inspection 1101420 · Voluntary Action Indicated (VAI) · Upplands Vasby

Key facts

Inspection ID 1101420
Firm Directa AB
FEI number 3004586882
Address Finvids Vag 8
City Upplands Vasby
Country Sweden
Fiscal year 2019
Inspection end date Sep 5, 2019
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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