FDA inspection

Themogenesis Corp.: FDA inspection ending Aug 29, 2011

FDA inspection 745069 · Voluntary Action Indicated (VAI) · Rancho Cordova, CA

Key facts

Inspection ID 745069
Firm Themogenesis Corp.
FEI number 1000123765
Address 2711 Citrus Rd
City Rancho Cordova
State CA
ZIP 95670
Country United States
Fiscal year 2011
Inspection end date Aug 29, 2011
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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