ZHEJIANG LEPU PHARMACEUTICAL CO., LTD.
FDA inspection history in TAIZHOU, China, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at TAIZHOU, China.
Cited most
Across all ZHEJIANG LEPU PHARMACEUTICAL CO. observations on file
- 21 CFR 211.142Warehousing procedures1
- 21 CFR 211.160General requirements1
The complete ZHEJIANG LEPU PHARMACEUTICAL CO. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
TAIZHOU, China
One Form 483 · 2018 · 2 observations
Latest: Form 483, Dec 7, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-12-07 | 483 Form 483 | TAIZHOU, China | 2 | $99 |
FEI number 3004414647 · most recent document Dec 7, 2018
About ZHEJIANG LEPU PHARMACEUTICAL CO., LTD.
How many FDA Form 483s has ZHEJIANG LEPU PHARMACEUTICAL CO., LTD. received?
FDA Intel has 1 Form 483 on file for ZHEJIANG LEPU PHARMACEUTICAL CO., LTD.; the most recent is dated Dec 7, 2018.
When was ZHEJIANG LEPU PHARMACEUTICAL CO., LTD. last inspected by FDA?
The most recent FDA inspection document on file for ZHEJIANG LEPU PHARMACEUTICAL CO., LTD. is a Form 483 dated Dec 7, 2018, for the site in TAIZHOU, China.
What did FDA cite at ZHEJIANG LEPU PHARMACEUTICAL CO., LTD.?
The regulations cited most in the observations on file for ZHEJIANG LEPU PHARMACEUTICAL CO., LTD. are 21 CFR 211.142 (Warehousing procedures), 1 time; 21 CFR 211.160 (General requirements), 1 time.