Tianjin Tianyao Pharmaceuticals Co., Ltd.
FDA inspection history in Tianjin, China, 2016 to 2019
- 2
- Form 483s
Every document, by year
- Form 483
2016: one Form 483; 2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Tianjin, China.
- 2016The longest 483 on file: 6 observations over 3 pages at Tianjin, China.
- 2019One Form 483, at Tianjin, China.
Cited most
Across all Tianjin Tianyao Pharmaceuticals Co. observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.192Production record review2
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.166Stability testing1
The complete Tianjin Tianyao Pharmaceuticals Co. file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Tianjin, China
Two Form 483s · 2016 to 2019 · 6 observations
Latest: Form 483, May 24, 2019 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-24 | 483 Form 483 | Tianjin, China | — | $99 |
| 2016-09-02 | 483 Form 483 | Tianjin, China | 6 | $99 |
Investigators on these documents
FEI number 3008256667 · most recent document May 24, 2019
About Tianjin Tianyao Pharmaceuticals Co., Ltd.
How many FDA Form 483s has Tianjin Tianyao Pharmaceuticals Co., Ltd. received?
FDA Intel has 2 Form 483s on file for Tianjin Tianyao Pharmaceuticals Co., Ltd.; the most recent is dated May 24, 2019.
When was Tianjin Tianyao Pharmaceuticals Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Tianjin Tianyao Pharmaceuticals Co., Ltd. is a Form 483 dated May 24, 2019, for the site in Tianjin, China.
What did FDA cite at Tianjin Tianyao Pharmaceuticals Co., Ltd.?
The regulations cited most in the observations on file for Tianjin Tianyao Pharmaceuticals Co., Ltd. are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times.