# SUZUKEN CO., LTD. OGUCHI CENTER – FDA Inspection, Jun 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/suzuken-co-ltd-oguchi-center/e3bedd18-8104-428e-b6f7-e5e4991c0d61
Source feed: FDA_Inspections

> FDA inspection 1058815 of SUZUKEN CO., LTD. OGUCHI CENTER, June 27, 2018. 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1058815
- Company Name: SUZUKEN CO., LTD. OGUCHI CENTER
- Inspection Date: 2018-06-27
- Project Area: Postmarket Assurance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Documents

- FDA Inspection 933588 - 2015-06-17
- [FDA Inspection 866643 - 2014-01-30](https://www.keypedia.com/records/fda_inspections/suzuken-co-ltd-oguchi-center/a654f6db-199e-49e1-b8cc-56bf392b7ce8)
- FDA Inspection 708074 - 2010-12-15

## Related Officers

- [Investigator](https://www.keypedia.com/people/stephen-r-souza/9b7af4df-f1cc-468d-9761-cee11d3c14fc)

Company: https://www.keypedia.com/companies/suzuken-co-ltd-oguchi-center/58c75523-8ed0-42f5-b961-1e2cd84980d4

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