FDA Investigator

Heika R Tait

Latest inspection on record: Spokane, United States, December 2014 · records back to 2008

Human Drugs

FDA inspection record · Last updated July 12, 2026

Overview

  • 52 inspections across 39 sites are on record.
  • 167 Form 483 observations are attributed to this investigator.
  • Most recent recorded activity is 2014-12-02.

At a glance

Inspections

52

Sites

39

Observations

167

Career since

Feb 2008

Recent inspections

Most recent inspections in the published record.

SiteDateCategoryForm 483
Jubilant HollisterStier LLC2 Dec 2014Human Drugs
Oregon Compounding Centers, Inc.28 Aug 2014Human DrugsView 483 →
Genentech, Inc.1 Jul 2014Human Drugs
HIKMA FARMACEUTICA (PORTUGAL), S.A28 Mar 2014Human DrugsView 483 →
Novartis Pharma S.A.S. - Centre de Biotechnologie18 Mar 2014Human Drugs

Sites inspected

Jubilant HollisterStier LLCSpokane, United States1 insp.
Oregon Compounding Centers, Inc.Wilsonville, United States1 insp.
Genentech, Inc.Hillsboro, United States1 insp.
HIKMA FARMACEUTICA (PORTUGAL), S.ATerrugem Snt, Portugal1 insp.

Co-investigators

Investigators who share inspections with this person.

Full investigator report

Get the verbatim findings behind Heika R Tait's 167 observations

Source 483 PDFs, verbatim observations, and how each site responded, so your team knows what they cite before they arrive.

  • New inspections and Form 483s, mapped to the CFR citation
  • Warning letter outcomes, and the citation patterns they repeat
  • Their co-investigators, so no surprises about who shows up on site