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Organization / Document #
DoD
Search Result: About 41710 results.

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  • 【Organization】DoD
  • 【Document #】HUD 24 CFR PART 9
  • ENFORCEMENT OF NON-DISCRIMINATION ON THE BASIS OF DISABILITY IN PROGRAMS OR ACTIVITIES CONDUCTED BY THE DEPARTMENT OF HOUSING AND URBAN DEVELOPMENT

  • 【Date】2018/4/1
  • 【Language】English
  • 【Status】Active
  • 【Organization】DoD
  • 【Document #】FDA 21 CFR PART 7
  • ENFORCEMENT POLICY

  • 【Date】2018/4/1
  • 【Language】English
  • 【Status】Active
  • 【Organization】DoD
  • 【Document #】DOT 23 CFR PART 620
  • ENGINEERING

  • 【Date】2018/4/1
  • 【Language】English
  • 【Status】Active
  • 【Organization】DoD
  • 【Document #】HUD 24 CFR PART 51
  • ENVIRONMENTAL CRITERIA AND STANDARDS

  • 【Date】2018/4/1
  • 【Language】English
  • 【Status】Active
  • 【Organization】DoD
  • 【Document #】DOT 23 CFR PART 771
  • ENVIRONMENTAL IMPACT AND RELATED PROCEDURES

  • 【Date】2018/4/1
  • 【Language】English
  • 【Status】Active
  • 【Organization】DoD
  • 【Document #】FDA 21 CFR PART 25
  • ENVIRONMENTAL IMPACT CONSIDERATIONS

  • 【Date】2018/4/1
  • 【Language】English
  • 【Status】Active
  • 【Organization】DoD
  • 【Document #】HUD 24 CFR PART 58
  • ENVIRONMENTAL REVIEW PROCEDURES FOR ENTITIES ASSUMING HUD ENVIRONMENTAL RESPONSIBILITIES

  • 【Date】2018/4/1
  • 【Language】English
  • 【Status】Active
  • 【Organization】DoD
  • 【Document #】FDA 21 CFR PART 807
  • ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES

  • 【Date】2018/4/1
  • 【Language】English
  • 【Status】Active
  • 【Organization】DoD
  • 【Document #】FDA 21 CFR PART 607
  • ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS

  • 【Date】2018/4/1
  • 【Language】English
  • 【Status】Active
  • 【Organization】DoD
  • 【Document #】FDA 21 CFR PART 1107
  • ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS

  • 【Date】2018/4/1
  • 【Language】English
  • 【Status】Active