# FDA Inspection 1020854 - Storz Medical America Inc - June 21, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/storz-medical-america-inc/45422f80-ed43-4a4e-b4db-a77999aefce3
Source feed: FDA_Inspections

> FDA Inspection 1020854 for Storz Medical America Inc on June 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020854
- Company Name: Storz Medical America Inc
- Inspection Date: 2017-06-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 911666 - 2015-01-28](https://www.globalkeysolutions.net/records/fda_inspections/storz-medical-america-inc/8a147c73-dcf6-4f97-8a19-c9789c7c9a39)

Company: https://www.globalkeysolutions.net/companies/storz-medical-america-inc/f12e2d05-a4e3-487d-a404-9aca21b7f0fc

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