# FDA 483 - Meito Sangyo Co., Ltd - April 04, 2025

Source: https://www.globalkeysolutions.net/records/483/meito-sangyo-co-ltd/b6779993-cfe8-4d91-8c97-e864d3432510

> FDA 483 for Meito Sangyo Co., Ltd on April 04, 2025. Product: other. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: Meito Sangyo Co., Ltd
- Inspection Date: 2025-04-04
- Product Type: other
- Office Name: Office of Inspections and Investigations
- Summary: Meito Sangyo Co., Ltd in Nagoya, Japan, a manufacturer of human food and dietary supplements, was cited for significant deficiencies during an FDA inspection. The firm failed to establish adequate specifications for dietary supplement ingredients and finished products, lacked master manufacturing records, and maintained incomplete batch production records. Additionally, the facility exhibited unsanitary conditions and equipment in disrepair, posing risks to product quality and safety.

## Related Officers

- [investigator](https://www.globalkeysolutions.net/people/diana-k-krepel/6dfec9cd-a933-4d1e-947c-cebb5891796c)

Company: https://www.globalkeysolutions.net/companies/meito-sangyo-co-ltd/c655667a-0b78-4f97-aca1-ac79144030aa

Office: https://www.globalkeysolutions.net/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8