Linda Galindo
FDA investigator
Appears on 4 documents from 2024 to 2026, mostly at sites in California. Most often cites receiving, in-process, and finished device acceptance (21 CFR 820.80).
- 4
- Documents on file
- 3.5
- Observations per 483
- 2024
- First seen
- 2026
- Most recent
What they cite most
From 14 observations- 21 CFR 820.80Receiving, in-process, and finished device acceptance4
- 21 CFR 820.75Process validation3
- 21 CFR 820.100(a)Corrective and preventive action2
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.25(b)Personnel1
- 21 CFR 820.50Purchasing controls1
Activity by year
2024: 2, 2025: 1, 2026: 1
Where
California 4
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Inspection history
4 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2026-02-12 | 483 Therapak CorporationFeb 12, 2026 · Claremont, California | Claremont, California | 2 | |
| 2025-08-21 | 483 Hoosier, IncAug 21, 2025 · Corona, California | Corona, California | 6 | |
| 2024-12-05 | 483 Rolenn Manufacturing IncDec 5, 2024 · Riverside, California | Riverside, California | 2 | |
| 2024-12-05 | 483 Rolenn Manufacturing IncDec 5, 2024 · Riverside, California | Riverside, California | 4 |
About this profile
What does Linda Galindo inspect?
Linda Galindo appears on 4 documents on file covering 3 sites, mostly in California.
What do they cite most often?
21 CFR 820.80 (receiving, in-process, and finished device acceptance), followed by 21 CFR 820.75 and 21 CFR 820.100(a).
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 Linda Galindo is dated Feb 12, 2026.