Zhejiang Peptides Biotech Co., Ltd.
FDA inspection history in Shaoxing 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 Shaoxing City, China.
Cited most
Across all Zhejiang Peptides Biotech Co. observations on file
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.180General requirements1
- 21 CFR 211.42Design and construction features1
The complete Zhejiang Peptides Biotech Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Shaoxing City, China
One Form 483 · 2023 · 3 observations
Latest: Form 483, Sep 8, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-09-08 | 483 Form 483 | Shaoxing City, China | 3 | $99 |
Investigators on these documents
FEI number 3015685285 · most recent document Sep 8, 2023
About Zhejiang Peptides Biotech Co., Ltd.
How many FDA Form 483s has Zhejiang Peptides Biotech Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Zhejiang Peptides Biotech Co., Ltd.; the most recent is dated Sep 8, 2023.
When was Zhejiang Peptides Biotech Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Peptides Biotech Co., Ltd. is a Form 483 dated Sep 8, 2023, for the site in Shaoxing City, China.
What did FDA cite at Zhejiang Peptides Biotech Co., Ltd.?
The regulations cited most in the observations on file for Zhejiang Peptides Biotech Co., Ltd. are 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times; 21 CFR 211.180 (General requirements), 1 time; 21 CFR 211.42 (Design and construction features), 1 time.