FDA inspection

Apheresis Technologies, Inc.: FDA inspection ending Oct 12, 1999

FDA inspection 673 · Official Action Indicated (OAI) · Palm Harbor, FL

Key facts

Inspection ID 673
Firm Apheresis Technologies, Inc.
FEI number 1000113717
Address 612 Florida Ave
City Palm Harbor
State FL
ZIP 34683-5459
Fiscal year 2000
Inspection end date Oct 12, 1999
Classification Official Action Indicated (OAI)
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(RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: 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Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act 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Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Postmarket Assurance: Med Devices|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth
Product type Devices
Warning letter UCM067856

At a glance

  • None Citations
  • 1–9 Posted citations
  • Yes Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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