Taylor L. Carmon
FDA investigator
Appears on 1 document from 2025, mostly at sites in Kentucky. Most often cites what are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me? (21 CFR 803.17).
- 1
- Documents on file
- 2.0
- Observations per 483
- 2025
- First seen
- 2025
- Most recent
What they cite most
From 2 observations- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.198(a)Complaint files1
Activity by year
2025: 1
Where
Kentucky 1
Often inspects with
Is Taylor L. Carmon coming to your site?
Our team writes custom reports before an inspection: what this investigator cites most, how they write it up, and how your site's history compares, in one brief you can circulate.
Ask about any investigator in Claude or ChatGPT with the AI connector.
Inspection history
1 document, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2025-07-02 | 483 MONOPRICE INCJul 2, 2025 · Hebron, Kentucky | Hebron, Kentucky | 2 |
About this profile
What does Taylor L. Carmon inspect?
Taylor L. Carmon appears on 1 document on file covering 1 site, mostly in Kentucky.
What do they cite most often?
21 CFR 803.17 (what are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), followed by 21 CFR 820.198(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 Taylor L. Carmon is dated Jul 2, 2025.