FDA inspection

Utak Laboratories Inc: FDA inspection ending Jan 24, 2018

FDA inspection 1052439 · Voluntary Action Indicated (VAI) · Valencia, CA

Key facts

Inspection ID 1052439
Firm Utak Laboratories Inc
FEI number 2022375
Address 25020 Avenue Tibbitts
City Valencia
State CA
ZIP 91355-3447
Fiscal year 2018
Inspection end date Jan 24, 2018
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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