# Feesers, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/feesers-inc/dfbe06a6-cc08-4202-86db-61ed1b86ba5d

> Inspection records and compliance data for Feesers, Inc. in Harrisburg, Pennsylvania. Access full analysis and detailed observations.

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## Details

- Name: Feesers, Inc.
- FEI Number: 2511306
- City: Harrisburg
- State: Pennsylvania
- Country Name: United States
- Address Line 1: 5561 Grayson Rd
- Zip Code: 17111

## Related Documents

- [FDA Inspection 1290970 - Feesers, Inc. - 2025-10-29](https://www.keypedia.com/records/fda_inspections/feesers-inc/0ab4f86e-b121-4148-abab-bc24d83dec5a) — source: FDA, date: October 29, 2025
- [FDA Inspection 1290970 - Feesers, Inc. - 2025-10-29](https://www.keypedia.com/records/fda_inspections/feesers-inc/53ba11a6-9442-4761-a260-8f840f8c6992) — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2025
- [FDA Inspection 1121183 - Feesers, Inc. - 2020-02-03](https://www.keypedia.com/records/fda_inspections/feesers-inc/bba8d4e5-a849-4ecf-93b4-08ac3ce9bc6b) — classification: No Action Indicated (NAI), source: FDA, date: February 3, 2020
- [FDA Inspection 1002897 - Feesers, Inc. - 2017-01-30](https://www.keypedia.com/records/fda_inspections/feesers-inc/f66891e1-18ea-467c-a5e1-f55723c97f2b) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2017
- [FDA Inspection 864624 - Feesers, Inc. - 2014-01-30](https://www.keypedia.com/records/fda_inspections/feesers-inc/a326b419-fb44-4f66-bb75-012cec6960dc) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2014
- [FDA Inspection 751294 - Feesers, Inc. - 2011-10-27](https://www.keypedia.com/records/fda_inspections/feesers-inc/f338d814-3ff1-49a6-b6a2-7d37c2cdf23a) — classification: No Action Indicated (NAI), source: FDA, date: October 27, 2011
- [FDA Inspection 541362 - Feesers, Inc. - 2008-10-08](https://www.keypedia.com/records/fda_inspections/feesers-inc/96a4e88f-d734-40c2-bf55-43e6e3c2a58e) — classification: No Action Indicated (NAI), source: FDA, date: October 8, 2008

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