Sunny Pharmtech Inc.
FDA inspection history in Taoyuan City, Taiwan, 2022
- 2
- Form 483s
Every document, by year
- Form 483
2022: two Form 483s.
The story so far
Built from the dates and citations on the documents themselves.
- 2022Two Form 483s, at Taoyuan City, Taiwan.
- 2022The longest 483 on file: 4 observations over 6 pages at Taoyuan City, Taiwan.
Cited most
Across all Sunny Pharmtech observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Sunny Pharmtech 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
Taoyuan City, Taiwan
Two Form 483s · 2022 · 8 observations
Latest: Form 483, Sep 29, 2022 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-09-29 | 483 Form 483 | Taoyuan City, Taiwan | 4 | $99 |
| 2022-04-15 | 483 Form 483 | Taoyuan City, Taiwan | 4 | $99 |
Investigators on these documents
FEI number 3013166187 · most recent document Sep 29, 2022
About Sunny Pharmtech Inc.
How many FDA Form 483s has Sunny Pharmtech Inc. received?
FDA Intel has 2 Form 483s on file for Sunny Pharmtech Inc.; the most recent is dated Sep 29, 2022.
When was Sunny Pharmtech Inc. last inspected by FDA?
The most recent FDA inspection document on file for Sunny Pharmtech Inc. is a Form 483 dated Sep 29, 2022, for the site in Taoyuan City, Taiwan.
What did FDA cite at Sunny Pharmtech Inc.?
The regulations cited most in the observations on file for Sunny Pharmtech Inc. are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.