15 U.S. Code § 2607 - Reporting and retention of information
Any person who manufactures, processes, or distributes in commerce any chemical substance or mixture shall maintain records of significant adverse reactions to health or the environment, as determined by the Administrator by rule, alleged to have been caused by the substance or mixture. Records of such adverse reactions to the health of employees shall be retained for a period of 30 years from the date such reactions were first reported to or known by the person maintaining such records. Any other record of such adverse reactions shall be retained for a period of five years from the date the information contained in the record was first reported to or known by the person maintaining the record. Records required to be maintained under this subsection shall include records of consumer allegations of personal injury or harm to health, reports of occupational disease or injury, and reports or complaints of injury to the environment submitted to the manufacturer, processor, or distributor in commerce from any source. Upon request of any duly designated representative of the Administrator, each person who is required to maintain records under this subsection shall permit the inspection of such records and shall submit copies of such records.
Any person who manufactures, processes, or distributes in commerce a chemical substance or mixture and who obtains information which reasonably supports the conclusion that such substance or mixture presents a substantial risk of injury to health or the environment shall immediately inform the Administrator of such information unless such person has actual knowledge that the Administrator has been adequately informed of such information.
For purposes of this section, the terms “manufacture” and “process” mean manufacture or process for commercial purposes.
 So in original.
2016—Subsec. (a)(2). Pub. L. 114–182, § 8(a)(1)(A), struck out concluding provisions which read as follows: “To the extent feasible, the Administrator shall not require under paragraph (1), any reporting which is unnecessary or duplicative.”
Subsec. (a)(2)(E). Pub. L. 114–182, § 19(g)(1), substituted “information” for “data”.
Subsec. (a)(3)(A)(ii)(I). Pub. L. 114–182, § 19(g)(2), substituted “, an order in effect under section 2603 or 2604(e) of this title, or a consent agreement under section 2603 of this title” for “or an order in effect under section 2604(e) of this title”.
Subsec. (a)(3)(C). Pub. L. 114–182, § 8(a)(1)(B), added subpar. (C).
Subsec. (a)(4) to (6). Pub. L. 114–182, § 8(a)(1)(C), added pars. (4) to (6).
Subsec. (b)(3) to (9). Pub. L. 114–182, § 8(a)(2), added pars. (3) to (9).
Subsec. (b)(10). Pub. L. 114–182, § 8(b), added par. (10).
“This Act may be cited as the ‘Asbestos Information Act of 1988’.
“Within 90 days after the date of the enactment of this Act [Oct. 31, 1988], any person who manufactured or processed, before the date of the enactment of this Act, asbestos or asbestos-containing material that was prepared for sale for use as surfacing material, thermal system insulation, or miscellaneous material in buildings (or whose corporate predecessor manufactured or processed such asbestos or material) shall submit to the Administrator of the Environmental Protection Agency the years of manufacture, the types or classes of product, and, to the extent available, other identifying characteristics reasonably necessary to identify or distinguish the asbestos or asbestos-containing material. Such person also may submit to the Administrator protocols for samples of asbestos and asbestos-containing material.
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