# JMS CO., LTD., Miyoshi Plant – FDA Inspection, Oct 25, 2024

Source: https://www.keypedia.com/records/fda_inspections/jms-co-ltd-miyoshi-plant/dcf92a76-b7ce-4df2-8252-8b233e7e784f
Source feed: FDA_Inspections

> FDA inspection 1253981 of JMS CO., LTD., Miyoshi Plant, October 25, 2024. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1253981
- Company Name: JMS CO., LTD., Miyoshi Plant
- Inspection Date: 2024-10-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## Related Documents

- FDA Inspection 947326 - 2015-09-11

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.keypedia.com/companies/jms-co-ltd-miyoshi-plant/5dbd708c-3719-4cbd-9726-17a110e8d06b

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