MicroBiopharm Japan Co., Ltd.
FDA inspection history in Iwata, Japan, 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 Iwata, Japan.
Cited most
Across all MicroBiopharm Japan Co. observations on file
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.150Distribution procedures1
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.188Batch production and control records1
The complete MicroBiopharm Japan Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Iwata, Japan
One Form 483 · 2019 · 5 observations
Latest: Form 483, Sep 13, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-09-13 | 483 Form 483 | Iwata, Japan | 5 | $99 |
Investigators on these documents
FEI number 3003992082 · most recent document Sep 13, 2019
About MicroBiopharm Japan Co., Ltd.
How many FDA Form 483s has MicroBiopharm Japan Co., Ltd. received?
FDA Intel has 1 Form 483 on file for MicroBiopharm Japan Co., Ltd.; the most recent is dated Sep 13, 2019.
When was MicroBiopharm Japan Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for MicroBiopharm Japan Co., Ltd. is a Form 483 dated Sep 13, 2019, for the site in Iwata, Japan.
What did FDA cite at MicroBiopharm Japan Co., Ltd.?
The regulations cited most in the observations on file for MicroBiopharm Japan Co., Ltd. are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.150 (Distribution procedures), 1 time.