Qingdao BAHEAL Pharmaceutical Co.,Ltd.

FDA inspection history in Qingdao, China, 2019

1
Form 483

Every document, by year

  • Form 483

2019: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2019One Form 483, at Qingdao, China.

Cited most

Across all Qingdao BAHEAL Pharmaceutical Co.,Ltd. observations on file

The complete Qingdao BAHEAL Pharmaceutical Co.,Ltd. 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
2019-12-06483 Form 483$99

Investigators on these documents

Joel D. Hustedt (1)

FEI number 3011922870 · most recent document Dec 6, 2019

About Qingdao BAHEAL Pharmaceutical Co.,Ltd.

How many FDA Form 483s has Qingdao BAHEAL Pharmaceutical Co.,Ltd. received?

FDA Intel has 1 Form 483 on file for Qingdao BAHEAL Pharmaceutical Co.,Ltd.; the most recent is dated Dec 6, 2019.

When was Qingdao BAHEAL Pharmaceutical Co.,Ltd. last inspected by FDA?

The most recent FDA inspection document on file for Qingdao BAHEAL Pharmaceutical Co.,Ltd. is a Form 483 dated Dec 6, 2019, for the site in Qingdao, China.

What did FDA cite at Qingdao BAHEAL Pharmaceutical Co.,Ltd.?

The regulations cited most in the observations on file for Qingdao BAHEAL Pharmaceutical Co.,Ltd. are 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times; 21 CFR 211.186 (Master production and control records), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.