# FDA Inspection 1013214 - AcquaMed Technologies Inc - May 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/acquamed-technologies-inc/3bd758b7-0cbb-427d-9fb5-e6de87a403b5
Source feed: FDA_Inspections

> FDA Inspection 1013214 for AcquaMed Technologies Inc on May 25, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013214
- Company Name: AcquaMed Technologies Inc
- Inspection Date: 2017-05-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 731750 - 2011-06-06](https://www.keypedia.com/records/fda_inspections/acquamed-technologies-inc/c54d10be-d26d-41f6-b157-c292d5b259c1)
- [FDA Inspection 731750 - 2011-06-06](https://www.keypedia.com/records/fda_inspections/acquamed-technologies-inc/2f8ba5d2-dfe8-4113-8ea2-fbcef98f895e)
- [FDA Inspection 731750 - 2011-06-06](https://www.keypedia.com/records/fda_inspections/acquamed-technologies-inc/3e63b77d-5484-4c9f-9637-d11707996687)

Company: https://www.keypedia.com/companies/acquamed-technologies-inc/efaddf85-0c87-4eec-b937-ed37139db534

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