Form 483 Remediation (Business Opportunities - Other Business Ads)
INNetAds > Business Opportunities > Other Business Ads
Item ID 2921366 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 : 17 June 2024 4:32 PM Number of Views: 56 | Item Owner : izielgroup1 Contact Email: (None) Contact Phone: (None) |
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2024-12-22 (0.729 sec)