Xiaoping Guan
FDA investigator
Appears on 1 document from 2016, mostly at sites in Italy. Most often cites general requirements (21 CFR 211.160).
- 1
- Documents on file
- 8.0
- Observations per 483
- 2016
- First seen
- 2016
- Most recent
What they cite most
From 8 observations- 21 CFR 211.160General requirements5
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.28Personnel responsibilities1
Activity by year
2016: 1
Where
Italy 1
Often inspects with
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Inspection history
1 document, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2016-07-15 | 483 CORDEN PHARMA SPAJul 15, 2016 · Caponago, Italy | Caponago, Italy | 8 |
About this profile
What does Xiaoping Guan inspect?
Xiaoping Guan appears on 1 document on file covering 1 site, mostly in Italy.
What do they cite most often?
21 CFR 211.160 (general requirements), followed by 21 CFR 211.192 and 21 CFR 211.22.
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 Xiaoping Guan is dated Jul 15, 2016.