# FDA Inspection 1095276 - Holymed Products Co., Ltd. - June 19, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/holymed-products-co-ltd/9aba731a-1f1d-443d-9574-888e86ab5f41
Source feed: FDA_Inspections

> FDA Inspection 1095276 for Holymed Products Co., Ltd. on June 19, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095276
- Company Name: Holymed Products Co., Ltd.
- Inspection Date: 2019-06-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 926644 - 2015-05-13](https://www.globalkeysolutions.net/records/fda_inspections/holymed-products-co-ltd/4ed0a578-7a52-4b12-8ecc-ba7d8a19c47f)

Company: https://www.globalkeysolutions.net/companies/holymed-products-co-ltd/b73b5c31-5d73-48da-95f7-0777092db0d2

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