# FDA Inspection 1221220 - AVIKO - September 14, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/aviko/fc39d5e5-a662-41fb-baa4-72514f6481b7/
Source feed: FDA_Inspections

> FDA Inspection 1221220 for AVIKO on September 14, 2023. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1221220
- Company Name: AVIKO
- Inspection Date: 2023-09-14
- Classification: No Action Indicated (NAI)
- Project Area: Foodborne Biological Hazards
- Product Type: Food/Cosmetics

## Related Documents

- [FDA Inspection 1221220 - 2023-09-14](https://www.globalkeysolutions.net/api/records/fda_inspections/aviko/79a15637-6654-4458-963f-a63f52bd40c9/)
- [FDA Inspection 1221220 - 2023-09-14](https://www.globalkeysolutions.net/api/records/fda_inspections/aviko/2ea15ee6-b53d-446a-90dc-50ba886b3678/)
- [FDA Inspection 1221220 - 2023-09-14](https://www.globalkeysolutions.net/api/records/fda_inspections/aviko/75848902-fb62-46b2-bf50-fb830d6d38d0/)

Company: https://www.globalkeysolutions.net/companies/aviko/2885cd54-adc9-4127-ad99-1aeeeac80d08