FDA inspection

Invivoscribe Technologies, Inc.: FDA inspection ending Nov 1, 2018

FDA inspection 1072296 · No Action Indicated (NAI) · San Diego, CA

Key facts

Inspection ID 1072296
Firm Invivoscribe Technologies, Inc.
FEI number 3014173060
Address 10222 Barnes Canyon Rd Bldg 100
City San Diego
State CA
ZIP 92121
Country United States
Fiscal year 2019
Inspection end date Nov 1, 2018
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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