Davinna Ligons
FDA investigator
Appears on 2 documents from 2017 to 2018, mostly at sites in California. Most often cites production record review (21 CFR 211.192).
- 2
- Documents on file
- 5.0
- Observations per 483
- 2017
- First seen
- 2018
- Most recent
What they cite most
From 8 observations- 21 CFR 211.192Production record review2
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.113Control of microbiological contamination1
Activity by year
2017: 1, 2018: 1
Where
California 1 · South Korea 1
Often inspects with
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Inspection history
2 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2018-03-16 | 483 Amgen, IncMar 16, 2018 · Thousand Oaks, California | Thousand Oaks, California | 7 | |
| 2017-11-17 | 483 Daewoong Pharmaceutical Co., Ltd. 35-14, Jeyakgongdan 4-Gil, Hyangnam-EupNov 17, 2017 · Hwaseong-Si, South Korea | Hwaseong-Si, South Korea | 3 |
About this profile
What does Davinna Ligons inspect?
Davinna Ligons appears on 2 documents on file covering 2 sites, mostly in California.
What do they cite most often?
21 CFR 211.192 (production record review), followed by 21 CFR 211.84 and 21 CFR 211.100.
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 Davinna Ligons is dated Mar 16, 2018.