FDA inspection

Curative Health Services: FDA inspection ending Mar 7, 2000

FDA inspection 20814 · No Action Indicated (NAI) · Lombard, IL

Key facts

Inspection ID 20814
Firm Curative Health Services
FEI number 1000114942
Address 1960 Springer Dr
City Lombard
State IL
ZIP 60148-6419
Fiscal year 2000
Inspection end date Mar 7, 2000
Classification No Action Indicated (NAI)
Project area Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality 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Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance|Blood and Blood Products|Drug Quality Assurance
Product type Biologics, 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.

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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