Martin M. Kimani
FDA investigator
Appears on 4 documents from 2025 to 2026, mostly at sites in Ohio. Most often cites production record review (21 CFR 211.192).
- 4
- Documents on file
- 5.5
- Observations per 483
- 2025
- First seen
- 2026
- Most recent
What they cite most
From 22 observations- 21 CFR 211.192Production record review4
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.166Stability testing2
- 21 CFR 211.194Laboratory records2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures2
Activity by year
2025: 3, 2026: 1
Where
Ohio 2 · Georgia 1 · Indiana 1
Often inspects with
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Inspection history
4 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2026-03-26 | 483 Newton Laboratories, Inc.Mar 26, 2026 · Conyers, Georgia | Conyers, Georgia | 3 | |
| 2025-12-23 | 483 Smithfield Biosciences, IncDec 23, 2025 · Cincinnati, Ohio | Cincinnati, Ohio | 6 | |
| 2025-07-14 | 483 Catalent Indiana LLCJul 14, 2025 · Bloomington, Indiana | Bloomington, Indiana | 6 | |
| 2025-03-04 | 483 KUTOL PRODUCTS COMPANYMar 4, 2025 · SHARONVILLE, Ohio | SHARONVILLE, Ohio | 7 |
About this profile
What does Martin M. Kimani inspect?
Martin M. Kimani appears on 4 documents on file covering 4 sites, mostly in Ohio.
What do they cite most often?
21 CFR 211.192 (production record review), followed by 21 CFR 211.100 and 21 CFR 211.166.
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 Martin M. Kimani is dated Mar 26, 2026.