# Kenover Marketing Corp., Bayonne, NJ – FDA Inspections

Source: https://www.keypedia.com/companies/kenover-marketing-corp/21165e19-e48c-489c-9d42-ca88dcabeb35

> Inspection records and compliance data for Kenover Marketing Corp. in Bayonne, New Jersey. 18 FDA inspections on record, 1 Form 483, last inspected May 27, 2025.

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## Details

- Name: Kenover Marketing Corp.
- FEI Number: 3004024934
- Address Line 1: 72 Hook Rd
- City: Bayonne
- State: New Jersey
- Zip Code: 07002
- Country Name: United States
- Address: 72 Hook Rd, Bayonne, New Jersey 07002, United States
- Country: United States

## Related Documents

- FDA Inspection 1272548 - Kenover Marketing Corp. - 2025-05-27 — source: FDA, date: May 27, 2025
- FDA Inspection 1272548 - Kenover Marketing Corp. - 2025-05-27 — classification: No Action Indicated (NAI), source: FDA, date: May 27, 2025
- FDA Inspection 1272548 - Kenover Marketing Corp. - 2025-05-27 — classification: No Action Indicated (NAI), source: FDA, date: May 27, 2025
- FDA Inspection 1272548 - Kenover Marketing Corp. - 2025-05-27 — classification: No Action Indicated (NAI), source: FDA, date: May 27, 2025
- FDA Inspection 1262854 - Kenover Marketing Corp. - 2025-03-04 — source: FDA, date: March 4, 2025
- FDA Inspection 1262854 - Kenover Marketing Corp. - 2025-03-04 — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2025
- [FDA Inspection 1222925 - Kenover Marketing Corp. - 2023-11-17](https://www.keypedia.com/records/fda_inspections/kenover-marketing-corp/d13abacf-9fd9-40c8-8759-427b7324fd0e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 17, 2023
- FDA Inspection 1220105 - Kenover Marketing Corp. - 2023-09-20 — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2023
- FDA Inspection 1177952 - Kenover Marketing Corp. - 2022-08-08 — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2022
- FDA Inspection 1123740 - Kenover Marketing Corp. - 2020-05-08 — classification: No Action Indicated (NAI), source: FDA, date: May 8, 2020

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