Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
FDA inspection history in Lianyungang, China, 2021
- 1
- Form 483
Every document, by year
- Form 483
2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at Lianyungang, China.
Cited most
Across all Chia Tai Tianqing Pharmaceutical Group Co. observations on file
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Chia Tai Tianqing Pharmaceutical Group Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Lianyungang, China
One Form 483 · 2021 · 1 observation
Latest: Form 483, Jan 14, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-01-14 | 483 Form 483 | Lianyungang, China | 1 | $99 |
Investigators on these documents
FEI number 3011860409 · most recent document Jan 14, 2021
About Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
How many FDA Form 483s has Chia Tai Tianqing Pharmaceutical Group Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Chia Tai Tianqing Pharmaceutical Group Co., Ltd.; the most recent is dated Jan 14, 2021.
When was Chia Tai Tianqing Pharmaceutical Group Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Chia Tai Tianqing Pharmaceutical Group Co., Ltd. is a Form 483 dated Jan 14, 2021, for the site in Lianyungang, China.
What did FDA cite at Chia Tai Tianqing Pharmaceutical Group Co., Ltd.?
The regulations cited most in the observations on file for Chia Tai Tianqing Pharmaceutical Group Co., Ltd. are 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.