# FDA Inspection 1046159 - Swaive Corporation - February 06, 2018

Source: https://www.keypedia.com/records/fda_inspections/swaive-corporation/7c1184f5-d4d5-456e-a5d6-c4f3091d0019
Source feed: FDA_Inspections

> FDA Inspection 1046159 for Swaive Corporation on February 06, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1046159
- Company Name: Swaive Corporation
- Inspection Date: 2018-02-06
- 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 1046159 - 2018-02-06](https://www.keypedia.com/records/fda_inspections/swaive-corporation/82f99efe-fbb9-4f56-80cf-325867812ed5)

Company: https://www.keypedia.com/companies/swaive-corporation/c8e94560-9249-4d41-81fe-45aed76fb58f

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