Lisa Whitt
FDA investigator
Appears on 3 documents from 2018 to 2020, mostly at sites in Texas. Most often cites written procedures; deviations (21 CFR 211.100).
- 3
- Documents on file
- 5.0
- Observations per 483
- 2018
- First seen
- 2020
- Most recent
What they cite most
From 15 observations- 21 CFR 211.100Written procedures; deviations3
- 21 CFR 211.160General requirements2
- 21 CFR 211.198Complaint files2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.42Design and construction features2
- 21 CFR 111.77What must you do if established specifications are not met?1
Activity by year
2018: 2, 2020: 1
Where
Texas 2 · Oklahoma 1
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2020-03-18 | 483 OHM Pharma, IncMar 18, 2020 · Mineral Wells, Texas | Mineral Wells, Texas | 1 | |
| 2018-09-13 | 483 Qualgen LLCSep 13, 2018 · Edmond, Oklahoma | Edmond, Oklahoma | 9 | |
| 2018-04-23 | 483 BioTE MedicalApr 23, 2018 · Irving, Texas | Irving, Texas | 5 |
About this profile
What does Lisa Whitt inspect?
Lisa Whitt appears on 3 documents on file covering 3 sites, mostly in Texas.
What do they cite most often?
21 CFR 211.100 (written procedures; deviations), followed by 21 CFR 211.160 and 21 CFR 211.198.
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 Lisa Whitt is dated Mar 18, 2020.