FDA inspection

Therapak Corporation: FDA inspection ending Apr 24, 2015

FDA inspection 925747 · No Action Indicated (NAI) · Claremont, CA

Key facts

Inspection ID 925747
Firm Therapak Corporation
FEI number 3010882984
Address 651 Wharton Dr
City Claremont
State CA
ZIP 91711
Country United States
Fiscal year 2015
Inspection end date Apr 24, 2015
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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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