# HOYA Corporation PENTAX Miyagi Factory, Kurihara, Japan – FDA Inspections

Source: https://www.keypedia.com/companies/hoya-corporation-pentax-miyagi-factory/581745ee-6ba6-4267-9528-b88f8c68388b

> Inspection records and compliance data for HOYA Corporation PENTAX Miyagi Factory in Kurihara. 5 FDA inspections on record, 2 Form 483s, last inspected August 03, 2023.

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## Details

- Name: HOYA Corporation PENTAX Miyagi Factory
- FEI Number: 3003782610
- Address Line 1: 30-2, Tsukidate
- City: Kurihara
- Country Name: Japan
- Address: 30-2, Tsukidate, Kurihara, Japan
- Country: Japan

## Related Documents

- [FDA Inspection 1214325 - HOYA Corporation PENTAX Miyagi Factory - 2023-08-03](https://www.keypedia.com/records/fda_inspections/hoya-corporation-pentax-miyagi-factory/443ad41d-2d8a-47a2-b936-49fafe277557) — source: FDA, date: August 3, 2023
- [FDA Inspection 1124077 - HOYA Corporation PENTAX Miyagi Factory - 2018-09-04](https://www.keypedia.com/records/fda_inspections/hoya-corporation-pentax-miyagi-factory/f2ee4415-d095-48d2-965b-c5052e4a1c52) — source: FDA, date: September 4, 2018
- [FDA Inspection 926494 - HOYA Corporation PENTAX Miyagi Factory - 2015-04-24](https://www.keypedia.com/records/fda_inspections/hoya-corporation-pentax-miyagi-factory/4b45504d-40d1-413a-95e6-854ba344f150) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 24, 2015
- [FDA Inspection 857579 - HOYA Corporation PENTAX Miyagi Factory - 2013-11-21](https://www.keypedia.com/records/fda_inspections/hoya-corporation-pentax-miyagi-factory/f6f72b63-9d67-4914-b3f7-69825b6459f7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 21, 2013
- FDA Inspection 857579 - HOYA Corporation PENTAX Miyagi Factory - 2013-11-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 21, 2013
- [FDA Inspection 705556 - HOYA Corporation PENTAX Miyagi Factory - 2010-12-16](https://www.keypedia.com/records/fda_inspections/hoya-corporation-pentax-miyagi-factory/a64af382-d217-45a2-bce9-96829fe79523) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 16, 2010

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