# FDA Inspection 1057908 - Anewmed Corporation - June 28, 2018

Source: https://www.keypedia.com/records/fda_inspections/anewmed-corporation/81c435ae-439d-44e8-9a17-9b7514431f0a
Source feed: FDA_Inspections

> FDA Inspection 1057908 for Anewmed Corporation on June 28, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1057908
- Company Name: Anewmed Corporation
- Inspection Date: 2018-06-28
- 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 1057908 - 2018-06-28](https://www.keypedia.com/records/fda_inspections/anewmed-corporation/76c52c5e-480e-4375-b3b8-58b088f48520)
- [FDA Inspection 993047 - 2016-10-18](https://www.keypedia.com/records/fda_inspections/anewmed-corporation/08e7d134-e8f0-4364-b87c-7d8d39a0a76e)

Company: https://www.keypedia.com/companies/anewmed-corporation/23f66c0f-3994-4b65-a9b3-7f4e0bd7fe0f

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