# FDA Inspection 939719 - Plastiape Spa - July 30, 2015

Source: https://www.keypedia.com/records/fda_inspections/plastiape-spa/61d0ca7a-0147-4a6c-b064-121bb74944b6
Source feed: FDA_Inspections

> FDA Inspection 939719 for Plastiape Spa on July 30, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 939719
- Company Name: Plastiape Spa
- Inspection Date: 2015-07-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/plastiape-spa/3be49df2-77d9-4c3e-85ba-8e4704ef2599

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