Nang Kuang Pharmaceutical Co. Ltd.
FDA inspection history in Tainan City, Taiwan, 2022 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2022: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022–24Two Form 483s, at Tainan City, Taiwan.
- 2022The longest 483 on file: 13 observations over 5 pages at Tainan City, Taiwan.
Cited most
Across all Nang Kuang Pharmaceutical Co. observations on file
- 21 CFR 211.113Control of microbiological contamination6
- 21 CFR 211.192Production record review3
- 21 CFR 211.42Design and construction features3
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160(b)General requirements1
The complete Nang Kuang Pharmaceutical 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
Tainan City, Taiwan
Two Form 483s · 2022 to 2024 · 19 observations
Latest: Form 483, Apr 2, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-04-02 | 483 Form 483 | Tainan City, Taiwan | 6 | $99 |
| 2022-06-16 | 483 Form 483 | Tainan City, Taiwan | 13 | $99 |
Investigators on these documents
FEI number 3004396086 · most recent document Apr 2, 2024
About Nang Kuang Pharmaceutical Co. Ltd.
How many FDA Form 483s has Nang Kuang Pharmaceutical Co. Ltd. received?
FDA Intel has 2 Form 483s on file for Nang Kuang Pharmaceutical Co. Ltd.; the most recent is dated Apr 2, 2024.
When was Nang Kuang Pharmaceutical Co. Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Nang Kuang Pharmaceutical Co. Ltd. is a Form 483 dated Apr 2, 2024, for the site in Tainan City, Taiwan.
What did FDA cite at Nang Kuang Pharmaceutical Co. Ltd.?
The regulations cited most in the observations on file for Nang Kuang Pharmaceutical Co. Ltd. are 21 CFR 211.113 (Control of microbiological contamination), 6 times; 21 CFR 211.192 (Production record review), 3 times; 21 CFR 211.42 (Design and construction features), 3 times.