Rong Wang
FDA investigator · also recorded as U. Ret Rong Wang, Es Rong Wang
Appears on 3 documents from 2019 to 2022, mostly at sites in Illinois. Most often cites general requirements (21 CFR 211.160).
- 3
- Documents on file
- 7.3
- Observations per 483
- 2019
- First seen
- 2022
- Most recent
What they cite most
From 22 observations- 21 CFR 211.160General requirements5
- 21 CFR 211.192Production record review4
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures3
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.100Written procedures; deviations1
Activity by year
2019: 1, 2022: 2
Where
Illinois 2 · France 1
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2022-10-14 | 483 Merck BiodevelopmentOct 14, 2022 · Martillac, France | Martillac, France | 10 | |
| 2022-01-14 | 483 Kashiv BioSciences, LLCJan 14, 2022 · Chicago, Illinois | Chicago, Illinois | 5 | |
| 2019-03-12 | 483 Kashiv BioSciences, LLCMar 12, 2019 · Chicago, Illinois | Chicago, Illinois | 7 |
About this profile
What does Rong Wang inspect?
Rong Wang appears on 3 documents on file covering 2 sites, mostly in Illinois.
What do they cite most often?
21 CFR 211.160 (general requirements), followed by 21 CFR 211.192 and 21 CFR 211.84.
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 Rong Wang is dated Oct 14, 2022.