# FDA Inspection 816590 - Fertipro N.V. - December 06, 2012

Source: https://www.keypedia.com/records/fda_inspections/fertipro-nv/3fd26ea1-9fcc-4330-a644-e4f8554c1f4c
Source feed: FDA_Inspections

> FDA Inspection 816590 for Fertipro N.V. on December 06, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 816590
- Company Name: Fertipro N.V.
- Inspection Date: 2012-12-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/fertipro-nv/9630423b-7c5f-422d-924e-7ffb0dcfceb9

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