FDA inspection

BIALEX: FDA inspection ending Dec 17, 2018

FDA inspection 1074860 · Voluntary Action Indicated (VAI) · Tucson, AZ

Key facts

Inspection ID 1074860
Firm BIALEX
FEI number 3011767425
Address 850 E Ohio St Ste 12
City Tucson
State AZ
ZIP 85714
Country United States
Fiscal year 2019
Inspection end date Dec 17, 2018
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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