Zhejiang Apeloa Biotechnology Co., Ltd.
FDA inspection history in Dongyang, 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 Dongyang, China.
Cited most
Across all Zhejiang Apeloa Biotechnology Co. observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Zhejiang Apeloa Biotechnology Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Dongyang, China
One Form 483 · 2023
Latest: Form 483, Sep 7, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-09-07 | 483 Form 483 | Dongyang, China | — | $99 |
Investigators on these documents
FEI number 3006003033 · most recent document Sep 7, 2023
About Zhejiang Apeloa Biotechnology Co., Ltd.
How many FDA Form 483s has Zhejiang Apeloa Biotechnology Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Zhejiang Apeloa Biotechnology Co., Ltd.; the most recent is dated Sep 7, 2023.
When was Zhejiang Apeloa Biotechnology Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Apeloa Biotechnology Co., Ltd. is a Form 483 dated Sep 7, 2023, for the site in Dongyang, China.
What did FDA cite at Zhejiang Apeloa Biotechnology Co., Ltd.?
The regulations cited most in the observations on file for Zhejiang Apeloa Biotechnology Co., Ltd. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.