Jamie P. Webb
FDA investigator
Appears on 2 documents from 2024 to 2026, mostly at sites in Tennessee. Most often cites 21 CFR 820.
- 2
- Documents on file
- 7.0
- Observations per 483
- 2024
- First seen
- 2026
- Most recent
What they cite most
From 14 observations- 21 CFR 8201
- 21 CFR 8301
- ISO 13485:2016 Clause 4.1.2What is the scope of this subpart?1
- ISO 13485:2016 Clause 7.3.9Definitions1
- 21 CFR 801.20(a)Label to bear a unique device identifier1
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
Activity by year
2024: 1, 2026: 1
Where
Tennessee 2
Often inspects with
Is Jamie P. Webb 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
2 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2026-02-12 | 483 Gobiquity, IncFeb 12, 2026 · Nashville, Tennessee | Nashville, Tennessee | 2 | |
| 2024-12-18 | 483 Variamed, LLCDec 18, 2024 · Chattanooga, Tennessee | Chattanooga, Tennessee | 12 |
About this profile
What does Jamie P. Webb inspect?
Jamie P. Webb appears on 2 documents on file covering 2 sites, mostly in Tennessee.
What do they cite most often?
21 CFR 820, followed by 21 CFR 830 and ISO 13485:2016 Clause 4.1.2.
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 Jamie P. Webb is dated Feb 12, 2026.