FDA inspection

Sterigenics U.S., LLC: FDA inspection ending Aug 26, 2003

FDA inspection 291229 · Voluntary Action Indicated (VAI) · Salt Lake City, UT

Key facts

Inspection ID 291229
Firm Sterigenics U.S., LLC
FEI number 1721676
Address 5725 W Harold Gatty Dr
City Salt Lake City
State UT
ZIP 84116-3763
Fiscal year 2003
Inspection end date Aug 26, 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|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med 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Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices|Drug Quality Assurance|Product Evaluation: Med Devices
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.

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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