FDA issued a Warning Letter to Artegraft, Inc. on 5/11/2010 as a result of this inspection.
FDA investigators audited the Artegraft - North Brunswick, NJ, United States facility and issued inspectional observations (via FDA 483) on 08 Mar 2010.
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- Category: Medical Devices & Rad Health
- Inspection end: 08 Mar 2010
- Location: North Brunswick, United States
- FEI: 1000121696