Evonik Rexim (Nanning) Pharmaceutical Co. Ltd.

FDA inspection history in Nanning, 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 Nanning, China.

Cited most

Across all Evonik Rexim (Nanning) Pharmaceutical Co. observations on file

The complete Evonik Rexim (Nanning) Pharmaceutical 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
2018-09-28483 Form 483$99

Investigators on these documents

Steven P. Donald (1)

FEI number 3004268442 · most recent document Sep 28, 2018

About Evonik Rexim (Nanning) Pharmaceutical Co. Ltd.

How many FDA Form 483s has Evonik Rexim (Nanning) Pharmaceutical Co. Ltd. received?

FDA Intel has 1 Form 483 on file for Evonik Rexim (Nanning) Pharmaceutical Co. Ltd.; the most recent is dated Sep 28, 2018.

When was Evonik Rexim (Nanning) Pharmaceutical Co. Ltd. last inspected by FDA?

The most recent FDA inspection document on file for Evonik Rexim (Nanning) Pharmaceutical Co. Ltd. is a Form 483 dated Sep 28, 2018, for the site in Nanning, China.

What did FDA cite at Evonik Rexim (Nanning) Pharmaceutical Co. Ltd.?

The regulations cited most in the observations on file for Evonik Rexim (Nanning) Pharmaceutical Co. Ltd. are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.