FDA inspection

Theradome, Inc.: FDA inspection ending Nov 20, 2017

FDA inspection 1035602 · No Action Indicated (NAI) · Pleasanton, CA

Key facts

Inspection ID 1035602
Firm Theradome, Inc.
FEI number 3008295459
Address 4900 Hopyard Rd Ste 100
City Pleasanton
State CA
ZIP 94588
Country United States
Fiscal year 2018
Inspection end date Nov 20, 2017
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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