Zedong Dong
FDA investigator
Appears on 3 documents from 2017 to 2020, most often at sites in China. Most often cites design controls (21 CFR 820.30).
- 3
- Documents on file
- 8.7
- Observations per 483
- 2017
- First seen
- 2020
- Most recent
What they cite most
From 26 observations- 21 CFR 820.30Design controls4
- 21 CFR 211.160General requirements3
- 21 CFR 211.192Production record review3
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.165Testing and release for distribution2
- 21 CFR 211.198Complaint files2
Activity by year
2017: 1, 2019: 1, 2020: 1
Where
China 1 · India 1 · Missouri 1
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2020-03-07 | 483 Solara Active Pharma Sciences LimitedMar 7, 2020 · Cuddalore, India | Cuddalore, India | 6 | |
| 2019-05-31 | 483 Zhejiang Huahai Pharmaceutical Co., Ltd.May 31, 2019 · Linhai, China | Linhai, China | 6 | |
| 2017-03-24 | 483 Meridian Medical Technologies, Inc. a Pfizer CompanyMar 24, 2017 · Brentwood, Missouri | Brentwood, Missouri | 14 |
About this profile
What does Zedong Dong inspect?
Zedong Dong appears on 3 documents on file covering 3 sites, most often in China.
What do they cite most often?
21 CFR 820.30 (design controls), followed by 21 CFR 211.160 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 Zedong Dong is dated Mar 7, 2020.