Full-scope SS304/316L fabrication of GMP-compliant process vessels, clean room structural mezzanines, and precision-polished product contact surfaces for a WHO-GMP pharma manufacturing line.
All product-contact surfaces required Ra ≤ 0.4 µm electropolish finish and full material traceability from mill certificate to final installation. Zero field welds allowed in classified clean room areas.
Every vessel, pipe spool, and structural element was fully fabricated and surface-finished in our facility. Pre-assembly was verified against clean room drawings before disassembly for transport and reinstallation.
Passed WHO-GMP audit with zero observations on fabrication quality. Client received drug manufacturing licence on first inspection attempt — a direct outcome of fabrication compliance.
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