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C.F.R. Title 21 Chapter I Subchapter H Part 822 Subpart D

Code of Federal Regulations · Subpart

Subpart D — Fda Review And Action

21 C.F.R. pt. 822, subpt. D

  • § 822.16 What Will You Consider In The Review Of My Submission?
  • § 822.17 How Long Will Your Review Of My Submission Take?
  • § 822.18 How Will I Be Notified Of Your Decision?
  • § 822.19 What Kinds Of Decisions May You Make?
  • § 822.20 What Are The Consequences If I Fail To Submit A Postmarket Surveillance Plan, My Plan Is Disapproved And I Fail To Submit A New Plan, Or I Fail To Conduct Surveillance In Accordance With My Approved Plan?
  • § 822.21 What Must I Do If I Want To Make Changes To My Postmarket Surveillance Plan After You Have Approved It?
  • § 822.22 What Recourse Do I Have If I Do Not Agree With Your Decision?
  • § 822.23 Is The Information In My Submission Considered Confidential?
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