Every FDA-Regulated Factory in One Connected Graph.

Cross-database analysis of the top 21 CFR Part 111 observations issued to capsule, gummy, powder, and botanical contract manufacturers, led by 21 CFR 111.75(a)(1) incoming ingredient identity testing and 21 CFR 111.205 Master Manufacturing Records.

Complete map of Texas supplement, food, chemical, pharmaceutical, and medical device facilities, including recent Form 483 observations, NAI clean-record co-packers, and warning letters.

Facility compliance records, cosmetic MoCRA registrations, supplement co-packers, and recent FDA ORA Pacific Southwest inspection findings across California.

How to vet skincare, serum, and OTC sunscreen contract manufacturers using FDA inspection records, recalls, import refusals, and MoCRA serious adverse event filings.

Ranking food and RTD beverage co-packers on sanitation (21 CFR 117.35), allergen controls, Foreign Supplier Verification (21 CFR 1.502), and Class I/II recall history.

Track foreign API, ingredient, supplement, and medical device factories whose shipments were detained without physical examination (DWPE) at U.S. ports of entry.