Chey Sorethan
FDA investigator
Appears on 1 document from 2020, mostly at sites in China. Most often cites sampling and testing of in-process materials and drug products (21 CFR 211.110).
- 1
- Documents on file
- 5.0
- Observations per 483
- 2020
- First seen
- 2020
- Most recent
What they cite most
From 5 observations- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.67Equipment cleaning and maintenance1
Activity by year
2020: 1
Where
China 1
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Inspection history
1 document, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2020-10-30 | 483 Shandong Anhong Pharmaceutical Co., Ltd.Oct 30, 2020 · Dezhou, China | Dezhou, China | 5 |
About this profile
What does Chey Sorethan inspect?
Chey Sorethan appears on 1 document on file covering 1 site, mostly in China.
What do they cite most often?
21 CFR 211.110 (sampling and testing of in-process materials and drug products), followed by 21 CFR 211.113 and 21 CFR 211.160.
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 Chey Sorethan is dated Oct 30, 2020.