FDA inspection

Midwest Sterilization Corp.: FDA inspection ending Apr 24, 2019

FDA inspection 1089902 · No Action Indicated (NAI) · Laredo, TX

Key facts

Inspection ID 1089902
Firm Midwest Sterilization Corp.
FEI number 3005012805
Address 12010 General Milton
City Laredo
State TX
ZIP 78045-1873
Fiscal year 2019
Inspection end date Apr 24, 2019
Classification No Action Indicated (NAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None 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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