# Artegraft, Inc., North Brunswick, NJ – FDA Inspections

Source: https://www.keypedia.com/companies/artegraft-inc/ea31640f-5897-4972-8d68-16ea7ca1d8eb

> Inspection records and compliance data for Artegraft, Inc. in North Brunswick, New Jersey. 8 FDA inspections on record (2 OAI), 3 Form 483s, last inspected June 25, 2026.

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## Details

- Name: Artegraft, Inc.
- FEI Number: 1000121696
- Address Line 1: 206 N Center Dr
- City: North Brunswick
- State: New Jersey
- Zip Code: 08902
- Country Name: United States
- Address: 206 N Center Dr, North Brunswick, New Jersey 08902, United States
- Country: United States

## Related Documents

- [483 - Artegraft, Inc. - 2026-06-25](https://www.keypedia.com/records/483/artegraft-inc/65dab17c-4e28-45eb-9fc2-eba8e27650ea) — source: FDA, date: June 25, 2026
- FDA Inspection 1325342 - Artegraft, Inc. - 2026-06-25 — source: FDA, date: June 25, 2026
- [FDA Inspection 1325342 - Artegraft, Inc. - 2026-06-25](https://www.keypedia.com/records/fda_inspections/artegraft-inc/042f5669-93b7-4704-a81e-2afc48e7f814) — source: FDA, date: June 25, 2026
- [483 - Artegraft, Inc. - 2025-04-16](https://www.keypedia.com/records/483/artegraft-inc/81d2d1fa-81af-44ce-bf7b-7db3dd1abcbf) — source: FDA, date: April 16, 2025
- [FDA Inspection 1235542 - Artegraft, Inc. - 2025-04-16](https://www.keypedia.com/records/fda_inspections/artegraft-inc/4ba57aee-568b-4a33-a2e7-c5fb71467292) — classification: Official Action Indicated (OAI), source: FDA, date: April 16, 2025
- FDA Inspection 1235542 - Artegraft, Inc. - 2025-04-16 — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2025
- FDA Inspection 1235542 - Artegraft, Inc. - 2025-04-16 — classification: Official Action Indicated (OAI), source: FDA, date: April 16, 2025
- FDA Inspection 1235542 - Artegraft, Inc. - 2025-04-16 — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2025
- [FDA Inspection 1202728 - Artegraft, Inc. - 2023-04-13](https://www.keypedia.com/records/fda_inspections/artegraft-inc/fc0624e3-73df-4afa-99ca-5e58fe389339) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 13, 2023
- FDA Inspection 1202728 - Artegraft, Inc. - 2023-04-13 — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2023
- FDA Inspection 1044392 - Artegraft, Inc. - 2018-02-16 — classification: No Action Indicated (NAI), source: FDA, date: February 16, 2018
- FDA Inspection 1044392 - Artegraft, Inc. - 2018-02-16 — classification: No Action Indicated (NAI), source: FDA, date: February 16, 2018

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## Related Officers

- [issuing_officer](https://www.keypedia.com/people/matthew-w-kyle/0f297104-ae6c-4fc4-a240-c84e5e907803)
- [Frank J. Marciniak](https://www.keypedia.com/people/frank-j-marciniak/6995351a-6afc-4056-9692-d4aeb711dd92)