Barbara Wright
FDA investigator
Appears on 6 documents from 2000 to 2025, most often at sites in Alabama. Most often cites general responsibilities of investigators (21 CFR 312.60).
- 6
- Documents on file
- 2.5
- Observations per 483
- 2000
- First seen
- 2025
- Most recent
What they cite most
From 5 observations- 21 CFR 312.60General responsibilities of investigators1
- 21 CFR 312.62Investigator recordkeeping and record retention1
Activity by year
2000: 1, 2007: 1, 2008: 1, 2009: 1, 2010: 1, 2025: 1
Where
Alabama 2 · Tennessee 2 · Indiana 1
Often inspects with
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Inspection history
6 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2025-10-25 | 483 Inotiv, IncOct 25, 2025 · West Lafayette, Indiana | West Lafayette, Indiana | 3 | |
| 2010-09-29 | Warning letter Warning letter, Sep 29, 2010Sep 29, 2010 | — | — | |
| 2009-01-29 | fda_correspondence Sarah Cannon Research InstituteJan 29, 2009 · Memphis, Tennessee | Memphis, Tennessee | — | |
| 2008-05-02 | 483 Howard W. Marker, M.D., Clinical InvestigatorMay 2, 2008 · Memphis, Tennessee | Memphis, Tennessee | 2 | |
| 2007-02-28 | Warning letter Capstone Clinical Trials, Inc.Feb 28, 2007 · Homewood, Alabama | Homewood, Alabama | — | |
| 2000-08-31 | Warning letter The Asthma and Allergy InstituteAug 31, 2000 · Mobile, Alabama | Mobile, Alabama | — |
About this profile
What does Barbara Wright inspect?
Barbara Wright appears on 6 documents on file covering 2 sites, most often in Alabama.
What do they cite most often?
21 CFR 312.60 (general responsibilities of investigators), followed by 21 CFR 312.62.
Can I read the observations?
Each document page previews the opening words of every observation. The full documents are available to buy, one at a time or together.
How current is this profile?
The most recent document on file for Barbara Wright is dated Oct 25, 2025.