# FDA Inspection 803735 - Aspide Medical - September 27, 2012

Source: https://www.keypedia.com/records/fda_inspections/aspide-medical/b46590c3-24f1-409d-b2bb-ad625d2a822f
Source feed: FDA_Inspections

> FDA Inspection 803735 for Aspide Medical on September 27, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803735
- Company Name: Aspide Medical
- Inspection Date: 2012-09-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 937908 - 2015-07-23](https://www.keypedia.com/records/fda_inspections/aspide-medical/4ea09773-ca63-430f-9632-f10d0ca4f2f0)
- [FDA Inspection 937908 - 2015-07-23](https://www.keypedia.com/records/fda_inspections/aspide-medical/ab0bc3c0-1139-4b86-8a89-714c791708b3)

Company: https://www.keypedia.com/companies/aspide-medical/9df266a6-110a-4ab5-a0b2-a7ae10e8d797

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