Kyongbo Pharmaceutical Co., Ltd.
FDA inspection history in Asan, South Korea, 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.
- 2019One Form 483, at Asan, South Korea.
Cited most
Across all Kyongbo Pharmaceutical Co. observations on file
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Kyongbo Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Asan, South Korea
One Form 483 · 2019 · 1 observation
Latest: Form 483, Dec 6, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-12-06 | 483 Form 483 | Asan, South Korea | 1 | $99 |
Investigators on these documents
FEI number 3003773799 · most recent document Dec 6, 2019
About Kyongbo Pharmaceutical Co., Ltd.
How many FDA Form 483s has Kyongbo Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Kyongbo Pharmaceutical Co., Ltd.; the most recent is dated Dec 6, 2019.
When was Kyongbo Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Kyongbo Pharmaceutical Co., Ltd. is a Form 483 dated Dec 6, 2019, for the site in Asan, South Korea.
What did FDA cite at Kyongbo Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Kyongbo Pharmaceutical Co., Ltd. are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.