# FDA Inspection 926048 - Endoplus - May 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/endoplus/5bd6d364-4965-4a04-99dc-d2448aebd67f
Source feed: FDA_Inspections

> FDA Inspection 926048 for Endoplus on May 19, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 926048
- Company Name: Endoplus
- Inspection Date: 2015-05-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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