Kellie R. Riggs
FDA investigator
Appears on 1 document from 2026, mostly at sites in Mississippi. Most often cites postmarketing reporting of adverse drug experiences (21 CFR 314.80(b)).
- 1
- Documents on file
- 4.0
- Observations per 483
- 2026
- First seen
- 2026
- Most recent
What they cite most
From 4 observations- 21 CFR 314.80(b)Postmarketing reporting of adverse drug experiences3
- 21 CFR 314.81(b)(2)Other postmarketing reports1
Activity by year
2026: 1
Where
Mississippi 1
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Inspection history
1 document, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2026-02-23 | 483 Misemer Pharmaceutical, IncFeb 23, 2026 · Ripley, Mississippi | Ripley, Mississippi | 4 |
About this profile
What does Kellie R. Riggs inspect?
Kellie R. Riggs appears on 1 document on file covering 1 site, mostly in Mississippi.
What do they cite most often?
21 CFR 314.80(b) (postmarketing reporting of adverse drug experiences), followed by 21 CFR 314.81(b)(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 Kellie R. Riggs is dated Feb 23, 2026.