# Holymed Products Co., Ltd. – FDA Inspection, Jun 19, 2019

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

> FDA inspection 1095276 of Holymed Products Co., Ltd., June 19, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 926644 - 2015-05-13

## Related Officers

- Issuing Officer

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

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