Kinkando CO., Ltd.
FDA inspection history in HONJO-SHI, Japan, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at HONJO-SHI, Japan.
Cited most
Across all Kinkando CO. observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
- 21 CFR 211.166Stability testing1
- 21 CFR 211.170Reserve samples1
The complete Kinkando CO. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
HONJO-SHI, Japan
One Form 483 · 2025 · 5 observations
Latest: Form 483, May 9, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-05-09 | 483 Form 483 | HONJO-SHI, Japan | 5 | $99 |
Investigators on these documents
FEI number 3004016987 · most recent document May 9, 2025
About Kinkando CO., Ltd.
How many FDA Form 483s has Kinkando CO., Ltd. received?
FDA Intel has 1 Form 483 on file for Kinkando CO., Ltd.; the most recent is dated May 9, 2025.
When was Kinkando CO., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Kinkando CO., Ltd. is a Form 483 dated May 9, 2025, for the site in HONJO-SHI, Japan.
What did FDA cite at Kinkando CO., Ltd.?
The regulations cited most in the observations on file for Kinkando CO., Ltd. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.160 (General requirements), 1 time.