Verified records and lab-supplied details never blend together.
Registration and matched regulatory records. Labs cannot edit or pay to improve them.
Methods, equipment, quality scope, capacity, turnaround, and commercial details. Always dated and attributed.
Outcomes are not facility grades.
No action indicated — FDA did not identify conditions warranting action in that inspection.
Voluntary action indicated — FDA documented observations for the facility to address voluntarily.
Official action indicated — FDA found conditions that may warrant official regulatory action.
Identifiers help match records.
We use the FDA Establishment Identifier (FEI) and Dun & Bradstreet D-U-N-S Number (DUNS) to keep sites distinct. Source gaps still occur, so “no record matched” never means “no record exists.”
Claiming never changes verified records.
Claims use exact-contact, corporate-domain, or manual review. Registration contacts stay private, and claiming is free.