CDER’s Framework for Regulatory Advanced Manufacturing Evaluation (FRAME) Initiative

Explore the FDA’s Regulatory Pharmaceutical Fellowship Program, a partnership with academia and industry, offering specialized training in regulatory science, policy, and drug development. Learn how to advance your career in the pharmaceutical field through this unique fellowship opportunity.

CGMP/Active Pharmaceutical Ingredient (API)/Adulterated

CGMP/Finished Pharmaceuticals/Adulterated

Pharmaceutical Quality/Manufacturing Standards (CGMP)

Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 1/14/2026
Short Title (70 char) US Specialty Formulations LLC. Allentown, PA. 483 issued 1/14/2026
FEI Number 3010680515
Firm Name US Specialty Formulations LLC
Record Type 483
State PA
Establishment Type Outsou

Record Date: 09/26/2025
Entity Name: Hetero Labs Limited (Warehouse)
FEI Number: 3040501127
Record Type: 483
Country: India
Establishment Type: Warehouse