# FDA Inspection 993047 - Anewmed Corporation - October 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/anewmed-corporation/08e7d134-e8f0-4364-b87c-7d8d39a0a76e
Source feed: FDA_Inspections

> FDA Inspection 993047 for Anewmed Corporation on October 18, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993047
- Company Name: Anewmed Corporation
- Inspection Date: 2016-10-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: 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 1057908 - 2018-06-28](https://www.keypedia.com/records/fda_inspections/anewmed-corporation/81c435ae-439d-44e8-9a17-9b7514431f0a)

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
