Pharmaceutical Manufacturing Duct Cleanliness

This is GMP/pharma HVAC. What cleanliness and documentation hold points do we need before install continues?

I'm checking pharmaceutical manufacturing duct cleanliness at [location]. I found: Duct is fabricated/installed without cleanliness protection, records, or pressure control awareness.. This is GMP/pharma HVAC. What cleanliness and documentation hold points do we need before install continues?

Insulation, Liner & Vapor Barrier 3rd Year RED

Stop if

Hold point on pharmaceutical manufacturing duct cleanliness: I have the location, photo, drawing/detail/spec/submittal, and what I checked. Who should verify before this gets covered, tested, started, labeled, rerouted, or turned over?

Watch out

Do not leave openings exposed or modify after cleaning without approval.

Check

room/grid/area
photo of condition
current drawing/detail/spec/submittal
what I already checked
what decision is needed

Say this to your foreman

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