Henan Lihua Pharmaceutical Co Ltd

FDA inspection history in Anyang, China, 2017 to 2021

2
Close-outs
1
Form 483

Every document, by year

  • Close-out
  • Form 483

2017: one Form 483; 2018: one close-out letter; 2021: one close-out letter.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2017–18One Form 483 and one close-out letter, at Anyang, China.
  2. 2021One close-out letter, at Anyang, China.

Cited most

Across all Henan Lihua Pharmaceutical Co observations on file

The complete Henan Lihua Pharmaceutical Co file.

All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$297

The price of the documents, added to your cart together

Sites

Documents

3 on file, newest first
DateDocumentPrice
2021-08-12Close-out Close-out letter$99
2018-06-12Close-out Close-out letter$99
2017-12-14483 Form 483$99

FEI number 3001164052 · most recent document Aug 12, 2021

About Henan Lihua Pharmaceutical Co Ltd

How many FDA Form 483s has Henan Lihua Pharmaceutical Co Ltd received?

FDA Intel has 1 Form 483 on file for Henan Lihua Pharmaceutical Co Ltd; the most recent is dated Dec 14, 2017.

When was Henan Lihua Pharmaceutical Co Ltd last inspected by FDA?

The most recent FDA inspection document on file for Henan Lihua Pharmaceutical Co Ltd is a Form 483 dated Dec 14, 2017, for the site in Anyang, China.

What did FDA cite at Henan Lihua Pharmaceutical Co Ltd?

The regulations cited most in the observations on file for Henan Lihua Pharmaceutical Co Ltd are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.194 (Laboratory records), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.