# American Beverage Corporation - Inspection Records

Source: https://www.keypedia.com/companies/american-beverage-corporation/660658b6-d8da-4dba-ba2e-886fb26a44b7

> Inspection records and compliance data for American Beverage Corporation in Verona, Pennsylvania. Access full analysis and detailed observations.

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## Details

- Name: American Beverage Corporation
- FEI Number: 2515935
- City: Verona
- State: Pennsylvania
- Country Name: United States
- Address Line 1: 1 Daily Way
- Zip Code: 15147

## Related Documents

- [FDA Inspection 1250180 - American Beverage Corporation - 2024-09-18](https://www.keypedia.com/records/fda_inspections/american-beverage-corporation/8a07f62c-b01b-4e4b-85db-e5acbf048edd) — source: FDA, date: September 18, 2024
- [FDA Inspection 1250180 - American Beverage Corporation - 2024-09-18](https://www.keypedia.com/records/fda_inspections/american-beverage-corporation/077c72ba-ec0b-4af9-a708-8c62abdcb023) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2024
- [FDA Inspection 1090072 - American Beverage Corporation - 2019-05-17](https://www.keypedia.com/records/fda_inspections/american-beverage-corporation/d3a7a125-1d0d-4273-aff1-bbd75703c0bc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 17, 2019
- [FDA Inspection 960328 - American Beverage Corporation - 2016-01-28](https://www.keypedia.com/records/fda_inspections/american-beverage-corporation/343be8b4-69d4-4152-9b21-db5854f7da26) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 28, 2016
- [FDA Inspection 568707 - American Beverage Corporation - 2009-02-24](https://www.keypedia.com/records/fda_inspections/american-beverage-corporation/04fbd982-6bbc-4276-b0d0-e10f06301604) — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2009
- [FDA Inspection 568707 - American Beverage Corporation - 2009-02-24](https://www.keypedia.com/records/fda_inspections/american-beverage-corporation/47163772-1db9-429b-9dc3-62f7b00c5c30) — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2009

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