Xianghong Jing
FDA investigator
Appears on 3 documents from 2016 to 2021, most often at sites in Austria. Most often cites who must register? (21 CFR 207.17).
- 3
- Documents on file
- 2.3
- Observations per 483
- 2016
- First seen
- 2021
- Most recent
What they cite most
From 7 observations- 21 CFR 207.17Who must register?1
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
- 21 CFR 211.56Sanitation1
- 21 CFR 211.80General requirements1
Activity by year
2016: 2, 2021: 1
Where
Austria 1 · Denmark 1 · Switzerland 1
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2021-12-17 | 483 Sandoz GmbHDec 17, 2021 · Kundl, Austria | Kundl, Austria | 5 | |
| 2016-07-08 | 483 FUJIFILM Diosynth Biotechnologies Denmark ApSJul 8, 2016 · Hillerod, Denmark | Hillerod, Denmark | 1 | |
| 2016-01-22 | 483 F. Hoffmann-La Roche AGJan 22, 2016 · Basel, Switzerland | Basel, Switzerland | 1 |
About this profile
What does Xianghong Jing inspect?
Xianghong Jing appears on 3 documents on file covering 3 sites, most often in Austria.
What do they cite most often?
21 CFR 207.17 (who must register?), followed by 21 CFR 211.100 and 21 CFR 211.113.
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 Xianghong Jing is dated Dec 17, 2021.