Orca1

FDA inspection

Ballard Medical Products: FDA inspection ending Nov 20, 2003

FDA inspection 302847 · Voluntary Action Indicated (VAI) · Draper, UT

Key facts

Inspection ID 302847
Firm Ballard Medical Products
FEI number 1719891
Address 12050 S Lone Peak Pkwy
City Draper
State UT
ZIP 84020-9414
Fiscal year 2004
Inspection end date Nov 20, 2003
Classification Voluntary Action Indicated (VAI)
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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|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med 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Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices|Drug Quality Assurance|Post Mrkt Surv & Epid: Human Drugs|Postmarket Assurance: Med Devices
Product type Devices, Drugs

At a glance

  • None 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.

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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