# Sugiyo USA INC, Anacortes, WA – FDA Inspections

Source: https://www.keypedia.com/companies/sugiyo-usa-inc/faef9fde-20bf-4bd7-be5f-668836d0327f

> Inspection records and compliance data for Sugiyo USA INC in Anacortes, Washington. 10 FDA inspections on record (1 OAI), 1 Form 483, last inspected March 23, 2026.

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## Details

- Name: Sugiyo USA INC
- FEI Number: 3023425
- Address Line 1: 3200 T Ave
- City: Anacortes
- State: Washington
- Zip Code: 98221
- Country Name: United States
- Address: 3200 T Ave, Anacortes, Washington 98221, United States
- Country: United States

## Related Documents

- FDA Inspection 1288011 - Sugiyo USA INC - 2026-03-23 — source: FDA, date: March 23, 2026
- FDA Inspection 1215357 - Sugiyo USA INC - 2023-08-10 — source: FDA, date: August 10, 2023
- [FDA Inspection 1134937 - Sugiyo USA INC - 2021-01-22](https://www.keypedia.com/records/fda_inspections/sugiyo-usa-inc/e4ad9122-c49f-4d58-bc53-2eb169d90937) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 22, 2021
- FDA Inspection 1134937 - Sugiyo USA INC - 2021-01-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 22, 2021
- [FDA Inspection 1121258 - Sugiyo USA INC - 2020-03-13](https://www.keypedia.com/records/fda_inspections/sugiyo-usa-inc/9690d16a-7c29-4c77-b7e6-52569027c1b2) — classification: Official Action Indicated (OAI), source: FDA, date: March 13, 2020
- [FDA Inspection 1047028 - Sugiyo USA INC - 2018-04-04](https://www.keypedia.com/records/fda_inspections/sugiyo-usa-inc/28dbdc67-3a9e-4c4f-8acc-7fa0b0ec9bef) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 4, 2018
- FDA Inspection 926248 - Sugiyo USA INC - 2015-05-14 — classification: No Action Indicated (NAI), source: FDA, date: May 14, 2015
- FDA Inspection 801120 - Sugiyo USA INC - 2012-09-07 — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2012
- FDA Inspection 767170 - Sugiyo USA INC - 2012-02-16 — classification: No Action Indicated (NAI), source: FDA, date: February 16, 2012
- FDA Inspection 679990 - Sugiyo USA INC - 2010-08-31 — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2010

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