FDA Warning Letter — BioLyte Laboratories, LLC

Case 603584 — FEI 3013171766

The FDA took a Warning Letter action against BioLyte Laboratories, LLC on Mar 18, 2021 (Grand Rapids, MI). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
BioLyte Laboratories, LLC
Date
Mar 18, 2021
Fiscal Year
2021
Product Type
Drugs
Center
CDER
Location
Grand Rapids, MI (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.