FDA Intel

Yiling Pharmaceutical Ltd.

FDA inspection history in Shijiazhuang, China, 2024 to 2025

1
Warning letter
1
Form 483

Every document, by year

  • Warning letter
  • Form 483

2024: one Form 483; 2025: one warning letter.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2024–25One Form 483 and one warning letter, at Shijiazhuang, China.

Cited most

Across all Yiling Pharmaceutical observations on file

  • 21 CFR 211.84
    Testing and approval or rejection of components, drug product containers, and closures
    2
  • 21 CFR 211.67
    Equipment cleaning and maintenance
    1

The complete Yiling Pharmaceutical file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2025-03-27Warning letter Warning letter$99
2024-10-11483 Form 483$99

Investigators on these documents

Patty P. Kaewussdangkul (1)

FEI number 3011640199 · most recent document Mar 27, 2025

About Yiling Pharmaceutical Ltd.

How many FDA Form 483s has Yiling Pharmaceutical Ltd. received?

FDA Intel has 1 Form 483 on file for Yiling Pharmaceutical Ltd.; the most recent is dated Oct 11, 2024.

When was Yiling Pharmaceutical Ltd. last inspected by FDA?

The most recent FDA inspection document on file for Yiling Pharmaceutical Ltd. is a Form 483 dated Oct 11, 2024, for the site in Shijiazhuang, China.

What did FDA cite at Yiling Pharmaceutical Ltd.?

The regulations cited most in the observations on file for Yiling Pharmaceutical Ltd. are 21 CFR 211.84 (Testing and approval or rejection of components, drug product containers, and closures), 2 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.

Has Yiling Pharmaceutical Ltd. received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for Yiling Pharmaceutical Ltd.; the most recent is dated Mar 27, 2025.