# FDA Inspection 1049647 - Anodyne Surgical - April 25, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/anodyne-surgical/9d91a5aa-3ba3-4063-b695-01f329724a05
Source feed: FDA_Inspections

> FDA Inspection 1049647 for Anodyne Surgical on April 25, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1049647
- Company Name: Anodyne Surgical
- Inspection Date: 2018-04-25
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1049647 - 2018-04-25](https://www.globalkeysolutions.net/records/fda_inspections/anodyne-surgical/aa126647-641f-40f7-9138-2b7a36b4a35f)

Company: https://www.globalkeysolutions.net/companies/anodyne-surgical/df342396-a85d-4f38-9fb1-45ea414a650d

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