FDA Inspection
GEODIS C/O PUREFRUIT/ TOPCOGEODIS C/O PUREFRUIT/ TOPCO – FDA Inspection, Sep 10, 2014
Record Details
This FDA Inspection record concerns GEODIS C/O PUREFRUIT/ TOPCO, with an inspection on September 10, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- GEODIS C/O PUREFRUIT/ TOPCO
- Inspection Date
- September 10, 2014
- Product Type
- Devices
View Company Profile
ID · 1835b23d-32b7-4324-9eb4-c87bd7da5604
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 894933
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.184DHR - not or inadequately maintained
Full citation text and observation details available on the Dashboard.
Other FDA inspections of GEODIS C/O PUREFRUIT/ TOPCO
2| Date | Classification | Office | Project area |
|---|---|---|---|
| July 10, 2024 | Not classified | Chicago District Office | |
| November 18, 2019 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
Other documents for GEODIS C/O PUREFRUIT/ TOPCO
- FDA Inspection 1246594 - 2024-07-10
- FDA Inspection 1111594 - 2019-11-18
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