Yi Wang
FDA investigator
Appears on 4 documents from 2023 to 2024, mostly at sites in California. Most often cites responsibilities of quality control unit (21 CFR 211.22).
- 4
- Documents on file
- 3.8
- Observations per 483
- 2023
- First seen
- 2024
- Most recent
What they cite most
From 15 observations- 21 CFR 211.22Responsibilities of quality control unit4
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.42Design and construction features2
- 21 CFR 211.142Warehousing procedures1
- 21 CFR 211.192Production record review1
Activity by year
2023: 3, 2024: 1
Where
California 3 · Pennsylvania 1
Often inspects with
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Inspection history
4 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2024-09-25 | 483 GlaxoSmithKline LLCSep 25, 2024 · Conshohocken, Pennsylvania | Conshohocken, Pennsylvania | 5 | |
| 2023-02-02 | 483 Genentech, Inc.Feb 2, 2023 · South San Francisco, California | South San Francisco, California | 4 | |
| 2023-01-24 | 483 Tanvex BioPharma USA, IncJan 24, 2023 · San Diego, California | San Diego, California | 3 | |
| 2023-01-16 | 483 Form 483 · FEI 3004575449Jan 16, 2023 · San Diego, California | San Diego, California | 3 |
About this profile
What does Yi Wang inspect?
Yi Wang appears on 4 documents on file covering 4 sites, mostly in California.
What do they cite most often?
21 CFR 211.22 (responsibilities of quality control unit), followed by 21 CFR 211.100 and 21 CFR 211.113.
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 Yi Wang is dated Sep 25, 2024.