# FDA Inspection 895349 - Venusa de Mexico S. de R.L de C.V - August 07, 2014

Source: https://www.keypedia.com/records/fda_inspections/venusa-de-mexico-s-de-rl-de-cv/bc941241-a7c1-457e-bc44-281e81abaae6
Source feed: FDA_Inspections

> FDA Inspection 895349 for Venusa de Mexico S. de R.L de C.V on August 07, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 895349
- Company Name: Venusa de Mexico S. de R.L de C.V
- Inspection Date: 2014-08-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 963075 - 2016-02-12](https://www.keypedia.com/records/fda_inspections/venusa-de-mexico-s-de-rl-de-cv/87294548-3bd8-4f66-9fc9-86ca24814ae1)

Company: https://www.keypedia.com/companies/venusa-de-mexico-s-de-rl-de-cv/746a7e6a-4d34-4f31-b895-e1e21e31a4a7

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