Three of D&A's seven processing rooms are dedicated to nutritional, food, and excipient work under FDA-registered conditions.
Every batch is verified against the customer's target particle size using calibrated sieve screens. We test multiple draws across the lot so the result reflects the full batch, not a single pull.
Bulk density is measured on the finished material so downstream operations like capsule filling, tableting, and bagging stay predictable.
Three of seven rooms are reserved for nutritionals, foods, and excipients. Chemical-side work runs in separate rooms, which prevents cross-contamination structurally rather than relying on cleaning procedures alone.
Every batch carries a documented record under ISO 9001:2015, traceable from raw material receipt through finished packaging.
Tyson Pritchard has personally processed over a thousand different materials. If yours isn't shown above, send the specification and we'll tell you whether it fits.
Email contact@dandagranulation.com or call 732-994-7480.
FDA-registered facility with dedicated rooms. Tell us the material and batch size.