Luis P. Torres
FDA investigator
Appears on 2 documents from 2025 to 2026, mostly at sites in California. Most often cites control of microbiological contamination (21 CFR 211.113(b)).
- 2
- Documents on file
- 9.0
- Observations per 483
- 2025
- First seen
- 2026
- Most recent
What they cite most
From 18 observations- 21 CFR 211.113(b)Control of microbiological contamination2
- 21 CFR 211.22(a)Responsibilities of quality control unit2
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures2
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.165(e)Testing and release for distribution1
Activity by year
2025: 1, 2026: 1
Where
California 1 · North Carolina 1
Often inspects with
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Inspection history
2 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2026-02-13 | 483 K.C. Pharmaceuticals, Inc.Feb 13, 2026 · Pomona, California | Pomona, California | 13 | |
| 2025-06-17 | 483 Glenmark Pharmaceuticals Inc.Jun 17, 2025 · Monroe, North Carolina | Monroe, North Carolina | 5 |
About this profile
What does Luis P. Torres inspect?
Luis P. Torres appears on 2 documents on file covering 2 sites, mostly in California.
What do they cite most often?
21 CFR 211.113(b) (control of microbiological contamination), followed by 21 CFR 211.22(a) and 21 CFR 211.84(d)(2).
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 Luis P. Torres is dated Feb 13, 2026.