Taizhou Xianju Pharmaceutical Co. Ltd.
FDA inspection history in Taizhou, China, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Taizhou, China.
Cited most
Across all Taizhou Xianju Pharmaceutical Co. observations on file
- 21 CFR 211.130Packaging and labeling operations1
- 21 CFR 211.67Equipment cleaning and maintenance1
- 21 CFR 211.80General requirements1
The complete Taizhou Xianju Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Taizhou, China
One Form 483 · 2017 · 3 observations
Latest: Form 483, Mar 31, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-03-31 | 483 Form 483 | Taizhou, China | 3 | $99 |
Investigators on these documents
FEI number 3012045665 · most recent document Mar 31, 2017
About Taizhou Xianju Pharmaceutical Co. Ltd.
How many FDA Form 483s has Taizhou Xianju Pharmaceutical Co. Ltd. received?
FDA Intel has 1 Form 483 on file for Taizhou Xianju Pharmaceutical Co. Ltd.; the most recent is dated Mar 31, 2017.
When was Taizhou Xianju Pharmaceutical Co. Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Taizhou Xianju Pharmaceutical Co. Ltd. is a Form 483 dated Mar 31, 2017, for the site in Taizhou, China.
What did FDA cite at Taizhou Xianju Pharmaceutical Co. Ltd.?
The regulations cited most in the observations on file for Taizhou Xianju Pharmaceutical Co. Ltd. are 21 CFR 211.130 (Packaging and labeling operations), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time; 21 CFR 211.80 (General requirements), 1 time.