Elisa M. Fleming
FDA investigator
Appears on 3 documents from 2011 to 2015, mostly at sites in Texas. Most often cites general requirements (21 CFR 211.160(b)).
- 3
- Documents on file
- 9.3
- Observations per 483
- 2011
- First seen
- 2015
- Most recent
What they cite most
From 28 observations- 21 CFR 211.160(b)General requirements3
- 21 CFR 211.42(a)Design and construction features3
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products2
- 21 CFR 211.188Batch production and control records2
- 21 CFR 211.198(a)Complaint files2
- 21 CFR 211.22(a)Responsibilities of quality control unit2
Activity by year
2011: 1, 2013: 1, 2015: 1
Where
Texas 2 · Oklahoma 1
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2015-02-13 | 483 Chemolee Lab CorporationFeb 13, 2015 · Irving, Texas | Irving, Texas | 13 | |
| 2013-12-20 | 483 Abrams Royal PharmacyDec 20, 2013 · Dallas, Texas | Dallas, Texas | 12 | |
| 2011-05-24 | 483 Mahard Egg Farms, IncMay 24, 2011 · SULPHUR, Oklahoma | SULPHUR, Oklahoma | 3 |
About this profile
What does Elisa M. Fleming inspect?
Elisa M. Fleming appears on 3 documents on file covering 3 sites, mostly in Texas.
What do they cite most often?
21 CFR 211.160(b) (general requirements), followed by 21 CFR 211.42(a) and 21 CFR 211.110(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 Elisa M. Fleming is dated Feb 13, 2015.