Kellie L. Thommes
FDA investigator
Appears on 4 documents from 2018 to 2025, mostly at sites in Minnesota. Most often cites exception from general requirements (21 CFR 50.23).
- 4
- Documents on file
- 3.7
- Observations per 483
- 2018
- First seen
- 2025
- Most recent
What they cite most
From 11 observations- 21 CFR 50.23Exception from general requirements2
- 21 CFR 56.111(a)(4)Criteria for IRB approval of research2
- 21 CFR 501
- 21 CFR 312.20(a)Requirement for an IND1
- 21 CFR 312.50General responsibilities of sponsors1
- 21 CFR 312.60General responsibilities of investigators1
Activity by year
2018: 1, 2019: 2, 2025: 1
Where
Minnesota 4
Often inspects with
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Inspection history
4 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2025-02-26 | 483 FDA Form 483 CSL Plasma Inc, Minneapolis, MN Feb 2025Feb 26, 2025 · Minneapolis, Minnesota | Minneapolis, Minnesota | 1 | |
| 2019-05-17 | Response Hennepin Healthcare System, Inc.May 17, 2019 · Minneapolis, Minnesota | Minneapolis, Minnesota | — | |
| 2019-04-26 | 483 Hennepin County Medical Center, Dept Of Emergency MedicineApr 26, 2019 · Minneapolis, Minnesota | Minneapolis, Minnesota | 6 | |
| 2018-08-23 | 483 Hennepin Healthcare System, Inc.Aug 23, 2018 · Minneapolis, Minnesota | Minneapolis, Minnesota | 4 |
About this profile
What does Kellie L. Thommes inspect?
Kellie L. Thommes appears on 4 documents on file covering 2 sites, mostly in Minnesota.
What do they cite most often?
21 CFR 50.23 (exception from general requirements), followed by 21 CFR 56.111(a)(4) and 21 CFR 50.
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 Kellie L. Thommes is dated Feb 26, 2025.