# FDA Inspection 932050 - Henry Schein Inc. - June 23, 2015

Source: https://www.keypedia.com/records/fda_inspections/henry-schein-inc/a2dc3f69-c49e-44e2-b45d-a6790cb7bbe5
Source feed: FDA_Inspections

> FDA Inspection 932050 for Henry Schein Inc. on June 23, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 932050
- Company Name: Henry Schein Inc.
- Inspection Date: 2015-06-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/henry-schein-inc/e2a35f07-783a-4f2d-b3c3-9313ee5e3885

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