FDA inspection

North American Science Associates, Inc.: FDA inspection ending Mar 12, 2004

FDA inspection 319201 · Voluntary Action Indicated (VAI) · Northwood, OH

Key facts

Inspection ID 319201
Firm North American Science Associates, Inc.
FEI number 1521876
Address 6750 Wales Rd
City Northwood
State OH
ZIP 43619-1012
Fiscal year 2004
Inspection end date Mar 12, 2004
Classification Voluntary Action Indicated (VAI)
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Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket 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Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|Postmarket Assurance: Med Devices|Drug Quality Assurance|Generic Drug Evaluation|New Drug Evaluation|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
  • 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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