# FDA Inspection 852386 - BIOSTER SPA - September 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/bioster-spa/0491bd70-5bd7-4bea-b65e-114df64b2c14
Source feed: FDA_Inspections

> FDA Inspection 852386 for BIOSTER SPA on September 12, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 852386
- Company Name: BIOSTER SPA
- Inspection Date: 2013-09-12
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 852386 - 2013-09-12](https://www.keypedia.com/records/fda_inspections/bioster-spa/e7fb8d26-bc5a-45fa-9d0a-3b7ed72c456c)

Company: https://www.keypedia.com/companies/bioster-spa/d39335bf-abcc-49c7-8923-b90f4adb0dc8

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