FDA inspection

Themogenesis Corp.: FDA inspection ending Mar 13, 2015

FDA inspection 917904 · No Action Indicated (NAI) · Rancho Cordova, CA

Key facts

Inspection ID 917904
Firm Themogenesis Corp.
FEI number 1000123765
Address 2711 Citrus Rd
City Rancho Cordova
State CA
ZIP 95670
Country United States
Fiscal year 2015
Inspection end date Mar 13, 2015
Classification No Action Indicated (NAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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