# FDA Inspection 1099706 - Tsubasa Industry Co., Ltd. - July 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/tsubasa-industry-co-ltd/a79f6d93-6df5-48ec-b46c-aa8d9993da6b
Source feed: FDA_Inspections

> FDA Inspection 1099706 for Tsubasa Industry Co., Ltd. on July 25, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1099706
- Company Name: Tsubasa Industry Co., Ltd.
- Inspection Date: 2019-07-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1099706 - 2019-07-25](https://www.keypedia.com/records/fda_inspections/tsubasa-industry-co-ltd/69c29628-2395-4fed-900a-6385ff77c9b8)
- [FDA Inspection 850596 - 2013-09-12](https://www.keypedia.com/records/fda_inspections/tsubasa-industry-co-ltd/4b524ca2-b632-4e6d-a610-1f6979fac4d1)
- [FDA Inspection 850596 - 2013-09-12](https://www.keypedia.com/records/fda_inspections/tsubasa-industry-co-ltd/c1dcd0e2-200e-4f94-ada6-060d1a40675c)

Company: https://www.keypedia.com/companies/tsubasa-industry-co-ltd/0782dc13-7090-41c2-9e99-2683003881a4

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7