FDA inspection

Victus, Inc.: FDA inspection ending Sep 29, 2004

FDA inspection 347316 · Voluntary Action Indicated (VAI) · Miami, FL

Key facts

Inspection ID 347316
Firm Victus, Inc.
FEI number 3002843564
Address 4918 SW 74th Ct
City Miami
State FL
ZIP 33155-4400
Fiscal year 2004
Inspection end date Sep 29, 2004
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|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological 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Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices|Foodborne Biological Hazard|Postmarket Assurance: Med Devices
Product type Devices, Food/Cosmetics

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
  • 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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