# FDA Inspection 975119 - IMEDICOM CO., LTD - June 02, 2016

Source: https://www.keypedia.com/records/fda_inspections/imedicom-co-ltd/62ccee36-470f-4778-8b8d-2120898c584c
Source feed: FDA_Inspections

> FDA Inspection 975119 for IMEDICOM CO., LTD on June 02, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 975119
- Company Name: IMEDICOM CO., LTD
- Inspection Date: 2016-06-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 975119 - 2016-06-02](https://www.keypedia.com/records/fda_inspections/imedicom-co-ltd/234adac8-a8e5-421b-ad15-d90f7c6ac44f)

Company: https://www.keypedia.com/companies/imedicom-co-ltd/8d6dbf58-ae04-4ef0-a1c3-9075f3af241a

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