Zhejiang Bamboo Pharmaceuticals Co.,Ltd

FDA inspection history in Shaoxing, 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.

  1. 2024One Form 483, at Shaoxing, China.

Cited most

Across all Zhejiang Bamboo Pharmaceuticals Co.,Ltd observations on file

The complete Zhejiang Bamboo Pharmaceuticals Co.,Ltd file.

All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.

$99

The documents one by one, while the file is prepared

See the documents

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Documents

1 on file, newest first
DateDocumentPrice
2024-09-27483 Form 483$99

FEI number 3019684157 · most recent document Sep 27, 2024

About Zhejiang Bamboo Pharmaceuticals Co.,Ltd

How many FDA Form 483s has Zhejiang Bamboo Pharmaceuticals Co.,Ltd received?

FDA Intel has 1 Form 483 on file for Zhejiang Bamboo Pharmaceuticals Co.,Ltd; the most recent is dated Sep 27, 2024.

When was Zhejiang Bamboo Pharmaceuticals Co.,Ltd last inspected by FDA?

The most recent FDA inspection document on file for Zhejiang Bamboo Pharmaceuticals Co.,Ltd is a Form 483 dated Sep 27, 2024, for the site in Shaoxing, China.

What did FDA cite at Zhejiang Bamboo Pharmaceuticals Co.,Ltd?

The regulations cited most in the observations on file for Zhejiang Bamboo Pharmaceuticals Co.,Ltd are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.