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- 【Organization】DoD
- 【Document #】FDA 21 CFR PART 1402
MANDATORY DECLASSIFICATION REVIEW
- 【Date】2018/4/1
- 【Language】English
- 【Status】Active
- 【Organization】DoD
- 【Document #】HUD 24 CFR PART 3280
MANUFACTURED HOME CONSTRUCTION AND SAFETY STANDARDS
- 【Date】2018/4/1
- 【Language】English
- 【Status】Active
- 【Organization】DoD
- 【Document #】HUD 24 CFR PART 3288
MANUFACTURED HOME DISPUTE RESOLUTION PROGRAM
- 【Date】2018/4/1
- 【Language】English
- 【Status】Active
- 【Organization】DoD
- 【Document #】HUD 24 CFR PART 3286
MANUFACTURED HOME INSTALLATION PROGRAM
- 【Date】2018/4/1
- 【Language】English
- 【Status】Active
- 【Organization】DoD
- 【Document #】HUD 24 CFR PART 3282
MANUFACTURED HOME PROCEDURAL AND ENFORCEMENT REGULATIONS
- 【Date】2018/4/1
- 【Language】English
- 【Status】Active
- 【Organization】DoD
- 【Document #】HUD 24 CFR PART 3284
MANUFACTURED HOUSING PROGRAM FEE
- 【Date】2018/4/1
- 【Language】English
- 【Status】Active
- 【Organization】DoD
- 【Document #】DOT 23 CFR PART 810
MASS TRANSIT AND SPECIAL USE HIGHWAY PROJECTS
- 【Date】2018/4/1
- 【Language】English
- 【Status】Active
- 【Organization】DoD
- 【Document #】FDA 21 CFR PART 860
MEDICAL DEVICE CLASSIFICATION PROCEDURES
- 【Date】2018/4/1
- 【Language】English
- 【Status】Active
- 【Organization】DoD
- 【Document #】FDA 21 CFR PART 810
MEDICAL DEVICE RECALL AUTHORITY
- 【Date】2018/4/1
- 【Language】English
- 【Status】Active
- 【Organization】DoD
- 【Document #】FDA 21 CFR PART 803
MEDICAL DEVICE REPORTING
- 【Date】2018/4/1
- 【Language】English
- 【Status】Active