Are you FDA certified?
Yes, the Keto-Mojo TD-4279 meter is an FDA-approved class II medical device for the in vitro self-testing of glucose and ketone levels, and it's suitable for testing for Type 1, Type 2, and gestational diabetes.
The meter is manufactured in an FDA-inspected and -approved establishment that also conforms to ISO:9001 manufacturing practices. The meter also conforms to ISO 15197:2013 standards.
Here are more specifics, in case you're interested:
- Keto-Mojo TD-4279 FDA device listing number:D126843
- Keto-Check, Inc FDA registration number: 10055466
- Manufacturing facility FDA establishment registration number 3004145393
- All our inventory is stored in an FDA-registered warehouse in Los Angeles. Registration number 12631797414
- Complete supply-chain custody is maintained throughout to assure you of genuine, quality products