Nuclear Regulatory Commission May 30, 2017 – Federal Register Recent Federal Regulation Documents
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List of Approved Spent Fuel Storage Casks: TN Americas, LLC, NUHOMS® EOS Dry Spent Fuel Storage System, Certificate of Compliance No. 1042
The U.S. Nuclear Regulatory Commission (NRC) is confirming the effective date of June 7, 2017, for the direct final rule that was published in the Federal Register on March 24, 2017. The direct final rule amended the NRC's spent fuel storage regulations by revising the ``List of approved spent fuel storage casks'' to add the TN Americas, LLC (TN Americas), NUHOMS[supreg] Extended Optimized Storage (EOS) Dry Spent Fuel Storage System as Certificate of Compliance (CoC) No. 1042.
Exelon Generation Company, LLC; Nine Mile Point Nuclear Station, Units 1 and 2
The U.S. Nuclear Regulatory Commission (NRC) is considering issuance of an amendment to Renewed Facility Operating License Nos. DPR-63 and NPF-69, issued to Exelon Generation Company, LLC, for operation of the Nine Mile Point Nuclear Station, Units 1 and 2, respectively. The proposed amendments would change the Emergency Action Level (EAL) HU1.5.
Exelon Generation Company, LLC; James A. FitzPatrick Nuclear Power Plant
The U.S. Nuclear Regulatory Commission (NRC) is considering issuance of an amendment to Renewed Facility Operating License No. DPR- 59, issued to Exelon Generation Company, LLC, for operation of the James A. FitzPatrick Nuclear Power Plant. The proposed amendment would change the Emergency Action Level (EAL) HU1.5.
Patient Release Program
On April 11, 2017, the U.S. Nuclear Regulatory Commission (NRC) solicited comments on its patient release program. The public comment period was originally scheduled to close on June 12, 2017. The NRC has decided to extend the public comment period to allow more time for members of the public to develop and submit their comments.
Information Collection: “10 CFR Part 35, Medical Use of Byproduct Material”
The U.S. Nuclear Regulatory Commission (NRC) has recently submitted a request for renewal of an existing collection of information to the Office of Management and Budget (OMB) for review. The information collection is entitled, ``10 CFR part 35, Medical Use of Byproduct Material.''
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