§ 40.169 Where is other information concerning the role of MROs and the verification process found in this regulation?
Wording first on file in the 2001 annual edition, superseded November 13, 2017.
You can find more information concerning the role of MROs in several sections of this part:
§ 40.3 - Definition.
§§ 40.47-40.49 - Correction of form and kit errors.
§ 40.67 - Role in direct observation and other atypical test situations.
§ 40.83 - Laboratory handling of fatal and correctable flaws.
§ 40.97 - Laboratory handling of test results and quantitative values.
§ 40.99 - Authorization of longer laboratory retention of specimens.
§ 40.101 - Relationship with laboratories; avoidance of conflicts of interest.
§ 40.105 - Notification of discrepancies in blind specimen results.
§ 40.171 - Request for test of split specimen.
§ 40.187 - Action concerning split specimen test results.
§ 40.193 - Role in “shy bladder” situations.
§ 40.195 - Role in cancelling tests.
§§ 40.199-40.203 - Documenting errors in tests.
§ 40.327 - Confidentiality and release of information.
§ 40.347 - Transfer of records.
§ 40.353 - Relationships with service agents.
Amendment history
3 distinct wordings on file since Oct. 1, 2001- [65 FR 79526, Dec. 19, 2000, as amended at 82 FR 52245, Nov. 13, 2017]
A new entry appears whenever the regulatory words change between government snapshots. Day-precise from the eCFR (2017 onward); before that, one snapshot per annual CFR edition (revised as of October 1). Bracketed citations are the Federal Register history printed with the section.