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August 23, 2025

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Month: August 2025

FDA Import Compliance & Customs Clearance Support Services – XPRO America


Posted on August 20, 2025 | Posted on admin | Leave a Comment on FDA Import Compliance & Customs Clearance Support Services – XPRO America

Successfully importing food, beverages, dietary supplements, cosmetics, and OTC products into the U.S. requires strict adherence to FDA import compliance and U.S. Customs clearance regulations. Failure to meet these requirements…

| Tagged customs broker FDA support, FDA cosmetic import compliance, FDA customs clearance, FDA customs clearance assistance, FDA customs clearance consultant, FDA customs documentation review, FDA entry compliance, FDA food import clearance, FDA hybrid product import, FDA import compliance, FDA import compliance consultant, FDA import compliance services, FDA import detention avoidance, FDA import entry requirements, FDA OTC import requirements, FDA Prior Notice consultant, FDA Prior Notice filing, FDA product detention support, FDA U.S. import guidance

FDA Cosmetics GMP Compliance & Quality Management Services – XPRO America


Posted on August 20, 2025 | Posted on admin | Leave a Comment on FDA Cosmetics GMP Compliance & Quality Management Services – XPRO America

Maintaining Good Manufacturing Practices (GMP) is essential for cosmetic companies that want to ensure product quality, safety, and regulatory compliance in the U.S. While the FDA does not require cosmetics…

FDA Adverse Event & Safety Reporting Compliance Services – XPRO America


Posted on August 20, 2025 | Posted on admin | Leave a Comment on FDA Adverse Event & Safety Reporting Compliance Services – XPRO America

Ensuring consumer safety is at the core of FDA regulations, and one of the most critical obligations for companies in the food, dietary supplement, cosmetic, and OTC product industries is…

| Tagged FDA adverse event audit, FDA adverse event consultant, FDA adverse event record management, FDA adverse event reporting, FDA adverse event reporting services, FDA adverse event submission, FDA audit preparation safety, FDA complaint handling, FDA compliance monitoring, FDA consumer safety reporting, FDA cosmetic adverse event reporting, FDA dietary supplement safety reporting, FDA MoCRA adverse event reporting, FDA MoCRA safety compliance, FDA OTC safety reporting, FDA safety compliance consultant, FDA safety recordkeeping, FDA safety reporting compliance, FDA supplement adverse event reporting

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Recent Posts

  • FDA Product Recall & Enforcement Guidance – XPRO AMERICA
  • FDA Compliance Monitoring for Renewals, Reviews & Updates – XPRO America
  • US FDA Agent Services for Foreign Manufacturers – XPRO AMERICA
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  • Premarket Approval (PMA) Applications for Class III Devices – XPRO AMERICA

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