Evelyn Wong
FDA investigator
Appears on 3 documents from 2016 to 2018, mostly at sites in California. Most often cites general requirements (21 CFR 211.160).
- 3
- Documents on file
- 11.3
- Observations per 483
- 2016
- First seen
- 2018
- Most recent
What they cite most
From 34 observations- 21 CFR 211.160General requirements4
- 21 CFR 211.165Testing and release for distribution4
- 21 CFR 211.192Production record review3
- 21 CFR 211.22Responsibilities of quality control unit3
- 21 CFR 211.42Design and construction features3
- 21 CFR 211.68Automatic, mechanical, and electronic equipment3
Activity by year
2016: 1, 2017: 1, 2018: 1
Where
California 3
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2018-06-29 | 483 B. Braun US Pharmaceutical Manufacturing LLCJun 29, 2018 · Irvine, California | Irvine, California | 8 | |
| 2017-05-26 | 483 Alliance Medical Products, Inc. (dba Siegfried Irvine)May 26, 2017 · Irvine, California | Irvine, California | 10 | |
| 2016-12-02 | 483 Auro Pha r mac i es I ncDec 2, 2016 · La Habra, California | La Habra, California | 16 |
About this profile
What does Evelyn Wong inspect?
Evelyn Wong appears on 3 documents on file covering 3 sites, mostly in California.
What do they cite most often?
21 CFR 211.160 (general requirements), followed by 21 CFR 211.165 and 21 CFR 211.192.
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 Evelyn Wong is dated Jun 29, 2018.