Deviation exposure
Visible duct debris found during an audit turns into a written deviation and a CAPA.
Pharmaceutical Manufacturing Facilities · Metro Atlanta, GA
Regulatory compliance, operational continuity and verified air quality — delivered with zero disruption to your pharma plants operation in Metro Atlanta, GA. Certified crews, engineered containment, and a documented report at handover.

Pharma plants in Metro Atlanta, GA share a specific set of failure modes in their HVAC systems. Below are the four we are called about most, and the standards that govern how each one has to be corrected and documented.
Visible duct debris found during an audit turns into a written deviation and a CAPA.
Shared air paths between suites move active ingredient dust where it does not belong.
Work that is not documented in advance stalls at the quality gate.
Cleaning must finish inside a planned turnaround, not extend it.
| Standard | How it applies |
|---|---|
| IICRC-certified source removal | Documented source removal and post-clean verification. |
| ASHRAE 62.1 | Ventilation performance for manufacturing and support areas. |
| EPA-registered chemistry | Only labeled antimicrobials, with SDS and application logs supplied. |
| OSHA 1910 | Lockout/tagout, confined space and PPE compliance throughout. |
Fire and smoke damper inspection and testing, grease-bearing exhaust cleaning and life-safety documentation prepared for AHJ and insurer review.
Every project follows the same sequence, whether it is one air handler or a full campus. Each step produces evidence that ends up in your handover report.
Every system is filmed before a brush touches it. The baseline footage sets the scope, identifies damage and closed dampers, and becomes the first half of your before/after record.
Work zones are isolated and held under negative pressure with HEPA-filtered machines, so debris leaves through the equipment instead of into the occupied building.
Rotary brushes, air whips and compressed-air tools release bonded debris while the vacuum holds continuous capture — source removal, not surface dusting.
Once the system is physically clean, labeled antimicrobial chemistry is applied to duct interiors, coils and pans, with product, dilution and dwell time logged.
Post-clean camera footage, airflow readings and particle counts are compiled into one report with technician credentials, standards applied and a floor-plan reference.
Yes. We supply the protocol, materials list, SDS sheets and technician credentials ahead of time so your quality group can raise change control, then work to that approved protocol with sign-off at each step.
Work stops in that zone, containment is extended, and we document the finding with photographs and location data before remediation continues. You get the finding in writing the same shift.
A dated record identifying each damper or hood by location, the condition found, the corrective action taken, and the technician who performed it. That is exactly the format of the binder we hand over.
It is photographed, logged as a deficiency with its location, and reported to you the same day. Repairs are quoted separately so nothing is done to life-safety equipment without your written approval.
Yes. Most commercial work in Metro Atlanta runs outside normal operating hours. We build the schedule around your occupancy and hand each area back clean and ready for use before your team returns.