TTY Biopharm Company Limited Lioudu Factory
FDA inspection history in Keelung City, Taiwan, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Keelung City, Taiwan.
Cited most
Across all TTY Biopharm Company Limited Lioudu Factory observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.170Reserve samples1
- 21 CFR 211.25Personnel qualifications1
- 21 CFR 211.52Washing and toilet facilities1
The complete TTY Biopharm Company Limited Lioudu Factory file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Keelung City, Taiwan
One Form 483 · 2022 · 4 observations
Latest: Form 483, Aug 30, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-08-30 | 483 Form 483 | Keelung City, Taiwan | 4 | $99 |
Investigators on these documents
FEI number 3015497585 · most recent document Aug 30, 2022
About TTY Biopharm Company Limited Lioudu Factory
How many FDA Form 483s has TTY Biopharm Company Limited Lioudu Factory received?
FDA Intel has 1 Form 483 on file for TTY Biopharm Company Limited Lioudu Factory; the most recent is dated Aug 30, 2022.
When was TTY Biopharm Company Limited Lioudu Factory last inspected by FDA?
The most recent FDA inspection document on file for TTY Biopharm Company Limited Lioudu Factory is a Form 483 dated Aug 30, 2022, for the site in Keelung City, Taiwan.
What did FDA cite at TTY Biopharm Company Limited Lioudu Factory?
The regulations cited most in the observations on file for TTY Biopharm Company Limited Lioudu Factory are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.170 (Reserve samples), 1 time; 21 CFR 211.25 (Personnel qualifications), 1 time.