# FDA Inspection 1096217 - Coretronic Projection (Kunshan) Corporation - June 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/coretronic-projection-kunshan-corporation/a51620ee-6881-4e52-9c90-f2cfb31ba298
Source feed: FDA_Inspections

> FDA Inspection 1096217 for Coretronic Projection (Kunshan) Corporation on June 14, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1096217
- Company Name: Coretronic Projection (Kunshan) Corporation
- Inspection Date: 2019-06-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/coretronic-projection-kunshan-corporation/fd23c70e-dd1c-4038-bbc8-5339b8deb1a1

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