Xiamen LP Pharmaceutical Co., Ltd.
FDA inspection history in Xiamen, China, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Xiamen, China.
Cited most
Across all Xiamen LP Pharmaceutical Co. observations on file
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Xiamen LP Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Xiamen, China
One Form 483 · 2022 · 2 observations
Latest: Form 483, Mar 4, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-03-04 | 483 Form 483 | Xiamen, China | 2 | $99 |
Investigators on these documents
FEI number 3013002864 · most recent document Mar 4, 2022
About Xiamen LP Pharmaceutical Co., Ltd.
How many FDA Form 483s has Xiamen LP Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Xiamen LP Pharmaceutical Co., Ltd.; the most recent is dated Mar 4, 2022.
When was Xiamen LP Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Xiamen LP Pharmaceutical Co., Ltd. is a Form 483 dated Mar 4, 2022, for the site in Xiamen, China.
What did FDA cite at Xiamen LP Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Xiamen LP Pharmaceutical Co., Ltd. are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.