ASANUMA CORPORATION

FDA inspection history in SAGAMIHARA, Japan, 2025 to 2026

1
Warning letter
1
Form 483

Every document, by year

  • Warning letter
  • Form 483

2025: one Form 483; 2026: one warning letter.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2025–26One Form 483 and one warning letter, at SAGAMIHARA, Japan.

Cited most

Across all ASANUMA observations on file

The complete ASANUMA file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2026-06-02Warning letter Warning letter$99
2025-02-28483 Form 483$99

Investigators on these documents

Matthew B. Casale (1)

FEI number 3010960168 · most recent document Jun 2, 2026

About ASANUMA CORPORATION

How many FDA Form 483s has ASANUMA CORPORATION received?

FDA Intel has 1 Form 483 on file for ASANUMA CORPORATION; the most recent is dated Feb 28, 2025.

When was ASANUMA CORPORATION last inspected by FDA?

The most recent FDA inspection document on file for ASANUMA CORPORATION is a Form 483 dated Feb 28, 2025, for the site in SAGAMIHARA, Japan.

What did FDA cite at ASANUMA CORPORATION?

The regulations cited most in the observations on file for ASANUMA CORPORATION are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.84(d)(2) (Testing and approval or rejection of components, drug product containers, and closures), 1 time.

Has ASANUMA CORPORATION received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for ASANUMA CORPORATION; the most recent is dated Jun 2, 2026.