YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY)
FDA inspection history in Taichung City, Taiwan, 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 Taichung City, Taiwan.
Cited most
Across all YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY) observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.192Production record review1
- 21 CFR 211.42Design and construction features1
The complete YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY) file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Taichung City, Taiwan
One Form 483 · 2019 · 7 observations
Latest: Form 483, Oct 22, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-10-22 | 483 Form 483 | Taichung City, Taiwan | 7 | $99 |
Investigators on these documents
FEI number 3002808536 · most recent document Oct 22, 2019
About YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY)
How many FDA Form 483s has YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY) received?
FDA Intel has 1 Form 483 on file for YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY); the most recent is dated Oct 22, 2019.
When was YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY) last inspected by FDA?
The most recent FDA inspection document on file for YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY) is a Form 483 dated Oct 22, 2019, for the site in Taichung City, Taiwan.
What did FDA cite at YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY)?
The regulations cited most in the observations on file for YUNG SHIN PHARM. IND. CO., LTD. (TAICHUNG YOUTH FACTORY) are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.186 (Master production and control records), 1 time.