# FDA Inspection 1032226 - Lebanon Agtegra - October 30, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/lebanon-agtegra/162ea12b-219c-4ed7-b811-4b30c26748f7
Source feed: FDA_Inspections

> FDA Inspection 1032226 for Lebanon Agtegra on October 30, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1032226
- Company Name: Lebanon Agtegra
- Inspection Date: 2017-10-30
- Classification: No Action Indicated (NAI)
- Project Area: Monitoring of Marketed Animal Drugs, Feed, and Devices
- Product Type: Veterinary
- Office Name: Center for Veterinary Medicine

## Related Documents

- [FDA Inspection 1032226 - 2017-10-30](https://www.globalkeysolutions.net/records/fda_inspections/lebanon-agtegra/1e6ba171-5b87-477a-a887-04115e9537eb)

Company: https://www.globalkeysolutions.net/companies/lebanon-agtegra/82907476-e0a4-4551-bffe-0a7029b1e0e4

Office: https://www.globalkeysolutions.net/offices/center-for-veterinary-medicine/7e30a309-56e4-4e7a-8b8b-e07674bb07b4
