FDA inspection

Midwest-Tek, Inc.: FDA inspection ending Apr 1, 2026

FDA inspection 1310382 · Voluntary Action Indicated (VAI) · New Albany, IN

Key facts

Inspection ID 1310382
Firm Midwest-Tek, Inc.
FEI number 3015525101
Address 4345 Security Pkwy
City New Albany
State IN
ZIP 47150
Country United States
Fiscal year 2026
Inspection end date Apr 1, 2026
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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