Human T-Lymphotropic Virus Type I (HTLV-I), Inactivated
Avioq Inc. certifies that the product was manufactured as per current Good Manufacturing Practices (cGMP), has passed Avioq Inc.’s internal quality control tests and inspections, and that the product meets specifications. Intended for laboratory research use or further manufacturing only. Not for use in human therapeutic or diagnostic applications.
75211 PD Rev 0
Avioq maintains an FDA (BLA) licensed and ISO 13485:2016 certified manufacturing facility in the United States.
Please provide all your product requirements and email us at this address for a prompt response: biomaterials@avioq.com