North China Pharmaceutical Huasheng Co., Ltd.

FDA inspection history in Shijiazhuang, China, 2018

1
Form 483

Every document, by year

  • Form 483

2018: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2018One Form 483, at Shijiazhuang, China.

Cited most

Across all North China Pharmaceutical Huasheng Co. observations on file

The complete North China Pharmaceutical Huasheng 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

Sites

Documents

1 on file, newest first
DateDocumentPrice
2018-08-10483 Form 483$99

Investigators on these documents

Niketa Patel (1)

FEI number 3003001488 · most recent document Aug 10, 2018

About North China Pharmaceutical Huasheng Co., Ltd.

How many FDA Form 483s has North China Pharmaceutical Huasheng Co., Ltd. received?

FDA Intel has 1 Form 483 on file for North China Pharmaceutical Huasheng Co., Ltd.; the most recent is dated Aug 10, 2018.

When was North China Pharmaceutical Huasheng Co., Ltd. last inspected by FDA?

The most recent FDA inspection document on file for North China Pharmaceutical Huasheng Co., Ltd. is a Form 483 dated Aug 10, 2018, for the site in Shijiazhuang, China.

What did FDA cite at North China Pharmaceutical Huasheng Co., Ltd.?

The regulations cited most in the observations on file for North China Pharmaceutical Huasheng Co., Ltd. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.63 (Equipment design, size, and location), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.