# C & E Canners, Inc., Hammonton, NJ – FDA Inspections

Source: https://www.keypedia.com/companies/c-e-canners-inc/8e06ec86-30bc-40af-8af4-17644eb4a1bf

> Inspection records and compliance data for C & E Canners, Inc. in Hammonton, New Jersey. 8 FDA inspections on record, last inspected May 18, 2026.

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## Details

- Name: C & E Canners, Inc.
- FEI Number: 2220031
- Address Line 1: 1249 Mays Landing Rd
- City: Hammonton
- State: New Jersey
- Zip Code: 08037
- Country Name: United States
- Address: 1249 Mays Landing Rd, Hammonton, New Jersey 08037, United States
- Country: United States

## Related Documents

- FDA Inspection 1319194 - C & E Canners, Inc. - 2026-05-18 — classification: No Action Indicated (NAI), source: FDA, date: May 18, 2026
- FDA Inspection 1218975 - C & E Canners, Inc. - 2023-09-20 — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2023
- FDA Inspection 1218975 - C & E Canners, Inc. - 2023-09-20 — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2023
- FDA Inspection 1115178 - C & E Canners, Inc. - 2020-01-16 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 16, 2020
- FDA Inspection 1115178 - C & E Canners, Inc. - 2020-01-16 — classification: No Action Indicated (NAI), source: FDA, date: January 16, 2020
- FDA Inspection 1055194 - C & E Canners, Inc. - 2018-02-14 — classification: No Action Indicated (NAI), source: FDA, date: February 14, 2018
- [FDA Inspection 936909 - C & E Canners, Inc. - 2015-08-07](https://www.keypedia.com/records/fda_inspections/c-e-canners-inc/a5fe930c-0911-4240-bd2c-1babe9ebef62) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 7, 2015
- FDA Inspection 936909 - C & E Canners, Inc. - 2015-08-07 — classification: No Action Indicated (NAI), source: FDA, date: August 7, 2015
- FDA Inspection 769734 - C & E Canners, Inc. - 2012-02-29 — classification: No Action Indicated (NAI), source: FDA, date: February 29, 2012
- FDA Inspection 672482 - C & E Canners, Inc. - 2010-07-20 — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2010

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