FDA inspection

Central Biomedia Inc: FDA inspection ending Feb 2, 2006

FDA inspection 412612 · Voluntary Action Indicated (VAI) · Lenexa, KS

Key facts

Inspection ID 412612
Firm Central Biomedia Inc
FEI number 1000119228
Address 9900 Pflumm Rd Ste 61
City Lenexa
State KS
ZIP 66215-1231
Fiscal year 2006
Inspection end date Feb 2, 2006
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices
Product type Devices

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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