Recordkeeping requirements for cGMP Regulations for Type A Medicated Feeds

Good Manufacturing Practice Regulations for Type A Medicated Articles

OMB: 0910-0154

IC ID: 5767

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Recordkeeping requirements for cGMP Regulations for Type A Medicated Feeds CVM
 
No Modified
 
Mandatory
 
21 CFR 226.42 21 CFR 226.58 21 CFR 226.80 21 CFR 226.102 21 CFR 226.110 21 CFR 226.115

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability

Health Consumer Health and Safety

 

65 49
   
Private Sector Businesses or other for-profits
 
   90 %

  Approved Program Change Due to New Statute Program Change Due to Agency Discretion Change Due to Adjustment in Agency Estimate Change Due to Potential Violation of the PRA Previously Approved
Annual Number of Responses for this IC 89,050 0 0 72,150 0 16,900
Annual IC Time Burden (Hours) 89,050 0 0 0 0 89,050
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

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