Fujian Genohope Biotech Ltd.
FDA inspection history in Putian, 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 Putian, China.
Cited most
Across all Fujian Genohope Biotech observations on file
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.105Equipment identification1
- 21 CFR 211.160General requirements1
- 21 CFR 211.80General requirements1
The complete Fujian Genohope Biotech file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Putian, China
One Form 483 · 2023 · 6 observations
Latest: Form 483, Jun 2, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-06-02 | 483 Form 483 | Putian, China | 6 | $99 |
Investigators on these documents
FEI number 3025263427 · most recent document Jun 2, 2023
About Fujian Genohope Biotech Ltd.
How many FDA Form 483s has Fujian Genohope Biotech Ltd. received?
FDA Intel has 1 Form 483 on file for Fujian Genohope Biotech Ltd.; the most recent is dated Jun 2, 2023.
When was Fujian Genohope Biotech Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Fujian Genohope Biotech Ltd. is a Form 483 dated Jun 2, 2023, for the site in Putian, China.
What did FDA cite at Fujian Genohope Biotech Ltd.?
The regulations cited most in the observations on file for Fujian Genohope Biotech Ltd. are 21 CFR 211.100 (Written procedures; deviations), 2 times; 21 CFR 211.105 (Equipment identification), 1 time; 21 CFR 211.160 (General requirements), 1 time.