Zhejiang Meimi Technology Co., Ltd.
FDA inspection history in Yiwu, China, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Yiwu, China.
Cited most
Across all Zhejiang Meimi Technology Co. observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.194(a)(4)Laboratory records1
- 21 CFR 211.196Distribution records1
- 21 CFR 211.22(c)Responsibilities of quality control unit1
The complete Zhejiang Meimi Technology Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Yiwu, China
One Form 483 · 2024 · 9 observations
Latest: Form 483, May 17, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-05-17 | 483 Form 483 | Yiwu, China | 9 | $99 |
Investigators on these documents
FEI number 3016802204 · most recent document May 17, 2024
About Zhejiang Meimi Technology Co., Ltd.
How many FDA Form 483s has Zhejiang Meimi Technology Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Zhejiang Meimi Technology Co., Ltd.; the most recent is dated May 17, 2024.
When was Zhejiang Meimi Technology Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Meimi Technology Co., Ltd. is a Form 483 dated May 17, 2024, for the site in Yiwu, China.
What did FDA cite at Zhejiang Meimi Technology Co., Ltd.?
The regulations cited most in the observations on file for Zhejiang Meimi Technology Co., Ltd. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.194(a)(4) (Laboratory records), 1 time.