# CPAC Equipment, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/cpac-equipment-inc/d0f113e5-d2b8-487e-8c48-5a9dd457979b

> Inspection records and compliance data for CPAC Equipment, Inc. in Leicester, New York. Access full analysis and detailed observations.

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## Details

- Name: CPAC Equipment, Inc.
- FEI Number: 2431273
- City: Leicester
- State: New York
- Country Name: United States
- Address Line 1: 2364 State Route 20a
- Zip Code: 14481

## Related Documents

- [483 - CPAC Equipment, Inc. - 2025-06-09](https://www.keypedia.com/records/483/cpac-equipment-inc/0732d1b8-841a-47a6-83e7-72c94ede77a7) — source: FDA, date: June 9, 2025
- [FDA Inspection 1274062 - CPAC Equipment, Inc. - 2025-06-09](https://www.keypedia.com/records/fda_inspections/cpac-equipment-inc/49281e81-94a4-4b7e-af30-ad856c2c96d5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 9, 2025
- [FDA Inspection 1274062 - CPAC Equipment, Inc. - 2025-06-09](https://www.keypedia.com/records/fda_inspections/cpac-equipment-inc/68a06453-2638-4b02-8bdf-6514a1ce686a) — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2025
- [FDA Inspection 1274062 - CPAC Equipment, Inc. - 2025-06-09](https://www.keypedia.com/records/fda_inspections/cpac-equipment-inc/4e17494d-7fdf-4418-9111-33289c5b827c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 9, 2025
- [FDA Inspection 1274062 - CPAC Equipment, Inc. - 2025-06-09](https://www.keypedia.com/records/fda_inspections/cpac-equipment-inc/49e949c2-505d-4b49-a4a4-12a62c726b9c) — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2025
- [FDA Inspection 1055114 - CPAC Equipment, Inc. - 2018-06-08](https://www.keypedia.com/records/fda_inspections/cpac-equipment-inc/11fa0ee5-eeec-4216-935f-b822a201ab4b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 8, 2018
- [FDA Inspection 1055114 - CPAC Equipment, Inc. - 2018-06-08](https://www.keypedia.com/records/fda_inspections/cpac-equipment-inc/34f3e968-a871-45a7-9839-a27edb7b251b) — classification: No Action Indicated (NAI), source: FDA, date: June 8, 2018

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