Yung Shin Pharm.Ind.(Kunshan) Co.,Ltd.
FDA inspection history in Suzhou, China, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Suzhou, China.
Cited most
Across all Yung Shin Pharm.Ind.(Kunshan) Co.,Ltd. observations on file
- 21 CFR 211.160(a)General requirements2
The complete Yung Shin Pharm.Ind.(Kunshan) Co.,Ltd. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Suzhou, China
One Form 483 · 2019 · 2 observations
Latest: Form 483, Mar 15, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-03-15 | 483 Form 483 | Suzhou, China | 2 | $99 |
Investigators on these documents
FEI number 3004079584 · most recent document Mar 15, 2019
About Yung Shin Pharm.Ind.(Kunshan) Co.,Ltd.
How many FDA Form 483s has Yung Shin Pharm.Ind.(Kunshan) Co.,Ltd. received?
FDA Intel has 1 Form 483 on file for Yung Shin Pharm.Ind.(Kunshan) Co.,Ltd.; the most recent is dated Mar 15, 2019.
When was Yung Shin Pharm.Ind.(Kunshan) Co.,Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Yung Shin Pharm.Ind.(Kunshan) Co.,Ltd. is a Form 483 dated Mar 15, 2019, for the site in Suzhou, China.
What did FDA cite at Yung Shin Pharm.Ind.(Kunshan) Co.,Ltd.?
The regulations cited most in the observations on file for Yung Shin Pharm.Ind.(Kunshan) Co.,Ltd. are 21 CFR 211.160(a) (General requirements), 2 times.