# FDA Inspection 820624 - Endoplus - February 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/endoplus/bc9e25c2-6cc6-4d54-9a1f-c19a315c2342
Source feed: FDA_Inspections

> FDA Inspection 820624 for Endoplus on February 26, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 820624
- Company Name: Endoplus
- Inspection Date: 2013-02-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: 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