Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd.
FDA inspection history in Jinhua, China, 2018 to 2023
- 2
- Form 483s
Every document, by year
- Form 483
2018: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Jinhua, China.
- 2023One Form 483, at Jinhua, China.
- 2023The longest 483 on file: 4 observations over 8 pages at Jinhua, China.
Cited most
Across all Zhejiang Jinhua Conba Bio-Pharm. Co. observations on file
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.25Personnel qualifications1
The complete Zhejiang Jinhua Conba Bio-Pharm. Co. file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Jinhua, China
Two Form 483s · 2018 to 2023 · 8 observations
Latest: Form 483, Aug 1, 2023 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-08-01 | 483 Form 483 | Jinhua, China | 4 | $99 |
| 2018-01-26 | 483 Form 483 | Jinhua, China | 4 | $99 |
Investigators on these documents
FEI number 3003663281 · most recent document Aug 1, 2023
About Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd.
How many FDA Form 483s has Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd. received?
FDA Intel has 2 Form 483s on file for Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd.; the most recent is dated Aug 1, 2023.
When was Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd. is a Form 483 dated Aug 1, 2023, for the site in Jinhua, China.
What did FDA cite at Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd.?
The regulations cited most in the observations on file for Zhejiang Jinhua Conba Bio-Pharm. Co., Ltd. are 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.160 (General requirements), 1 time.