# FDA Inspection 894933 - GEODIS C/O PUREFRUIT/ TOPCO - September 10, 2014

Source: https://www.keypedia.com/records/fda_inspections/geodis-co-purefruit-topco/1835b23d-32b7-4324-9eb4-c87bd7da5604
Source feed: FDA_Inspections

> FDA Inspection 894933 for GEODIS C/O PUREFRUIT/ TOPCO on September 10, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 894933
- Company Name: GEODIS C/O PUREFRUIT/ TOPCO
- Inspection Date: 2014-09-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1111594 - 2019-11-18](https://www.keypedia.com/records/fda_inspections/geodis-co-purefruit-topco/d2c0fe90-beb2-42ba-9cfb-641f1e882f1e)

Company: https://www.keypedia.com/companies/geodis-co-purefruit-topco/a2152f9b-6a82-4a1e-b1c9-c9be3212ce5c

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