# FDA Inspection 926048 - Endoplus - May 19, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/endoplus/fb5ddfe5-2517-4b86-b6b0-8dd5a69c66de/
Source feed: FDA_Inspections

> FDA Inspection 926048 for Endoplus on May 19, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 926048
- Company Name: Endoplus
- Inspection Date: 2015-05-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/endoplus/9145c0d3-d056-483a-93f5-f588957afd2a

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