Guang’an Kingday Pharma & Chem Co., Ltd.

FDA inspection history in Guangan, 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 Guangan, China.

Cited most

Across all Guang’an Kingday Pharma & Chem Co. observations on file

The complete Guang’an Kingday Pharma & Chem Co. 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
2024-05-24483 Form 483$99

FEI number 3009846816 · most recent document May 24, 2024

About Guang’an Kingday Pharma & Chem Co., Ltd.

How many FDA Form 483s has Guang’an Kingday Pharma & Chem Co., Ltd. received?

FDA Intel has 1 Form 483 on file for Guang’an Kingday Pharma & Chem Co., Ltd.; the most recent is dated May 24, 2024.

When was Guang’an Kingday Pharma & Chem Co., Ltd. last inspected by FDA?

The most recent FDA inspection document on file for Guang’an Kingday Pharma & Chem Co., Ltd. is a Form 483 dated May 24, 2024, for the site in Guangan, China.

What did FDA cite at Guang’an Kingday Pharma & Chem Co., Ltd.?

The regulations cited most in the observations on file for Guang’an Kingday Pharma & Chem Co., Ltd. are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.