Ningbo Shuangcheng Pharmaceutical Co., Ltd
FDA inspection history in Cixi city, China, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Cixi city, China.
Cited most
Across all Ningbo Shuangcheng Pharmaceutical Co. observations on file
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Ningbo Shuangcheng Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Cixi city, China
One Form 483 · 2023 · 2 observations
Latest: Form 483, Nov 3, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-11-03 | 483 Form 483 | Cixi city, China | 2 | $99 |
FEI number 3014148045 · most recent document Nov 3, 2023
About Ningbo Shuangcheng Pharmaceutical Co., Ltd
How many FDA Form 483s has Ningbo Shuangcheng Pharmaceutical Co., Ltd received?
FDA Intel has 1 Form 483 on file for Ningbo Shuangcheng Pharmaceutical Co., Ltd; the most recent is dated Nov 3, 2023.
When was Ningbo Shuangcheng Pharmaceutical Co., Ltd last inspected by FDA?
The most recent FDA inspection document on file for Ningbo Shuangcheng Pharmaceutical Co., Ltd is a Form 483 dated Nov 3, 2023, for the site in Cixi city, China.
What did FDA cite at Ningbo Shuangcheng Pharmaceutical Co., Ltd?
The regulations cited most in the observations on file for Ningbo Shuangcheng Pharmaceutical Co., Ltd are 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.