Form 483 Remediation (Business Opportunities - Other Business Ads)

Item ID 2553084 in Category: Business Opportunities - Other Business Ads

Form 483 Remediation
Medical device manufacturers receive observations (Form 483) and / or warning letters on completion of USFDA Audit. The document outlines any violations of Good Manufacturing Practices (GMP’s) such as the facility, equipment, processes, controls, products, employee practices or records.IZiel has successfully assisted medical device companies to resolve these observations with efficiency and accuracy.
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Target State: All States Target City : All Cities Last Update : Feb 29, 2024 3:27 AM Number of Views: 50	Item Owner : izielgroup1 Contact Email: (None) Contact Phone: (None)

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2024-12-24 (0.386 sec)