NIOSH Conformity Assessment Letter to Manufacturers, CA 2020-1030 - Requirements and Responsibilities of Approval Holders and Assignees in NIOSH Approved Respirator Private Labeling and Private Packaging Arrangements

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NIOSH Conformity Assessment Letter to Manufacturers, CA 2020-1030 - Requirements and Responsibilities of Approval Holders and Assignees in NIOSH Approved Respirator Private Labeling and Private Packaging Arrangements

06/25/2020

[PDF-172.52 KB]

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Description:

NIOSH Approval Holders and those they designate as Private Label (PL) entities have obligations when an extension of approval request for a private label is granted. All of the requirements listed below are well documented in NIOSH Standard Application Procedures.
Document Type:

Report
CIO:

NIOSH
Division:

NIOSH_NPPTL
Collection(s):

Historical CDC.gov Content
Main Document Checksum:

[+]

urn:sha256:de53a9aec680f35d7c84244e4f749a2bae02f257758ce7d15cd762e97e4e7b4e
Download URL:

https://stacks.cdc.gov/view/cdc/137552/cdc_137552_DS1.pdf
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NIOSH Conformity Assessment Letter to Manufacturers, CA 2020-1030 - Requirements and Responsibilities of Approval Holders and Assignees in NIOSH Approved Respirator Private Labeling and Private Packaging Arrangements

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