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FDA inspection

Sterigenics US LLC: FDA inspection ending Jan 9, 2003

FDA inspection 252883 · Voluntary Action Indicated (VAI) · Gurnee, IL

Key facts

Inspection ID 252883
Firm Sterigenics US LLC
FEI number 3000215273
Address 1003 Lakeside Dr
City Gurnee
State IL
ZIP 60031-2489
Fiscal year 2003
Inspection end date Jan 9, 2003
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug 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Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation|Drug Quality Assurance|Generic Drug Evaluation
Product type Devices, Drugs

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
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

Other inspections at this establishment

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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