FDAFDA Registered FacilityDEADEA Schedule II–V LicensedVAWDVAWD AccreditedcGMPcGMP CompliantUSP 797USP 797 / 800 CompliantISO 9001ISO 9001:2015 CertifiedDSCSADSCSA Track & TracePDMAPDMA CompliantFDAFDA Registered FacilityDEADEA Schedule II–V LicensedVAWDVAWD AccreditedcGMPcGMP CompliantUSP 797USP 797 / 800 CompliantISO 9001ISO 9001:2015 CertifiedDSCSADSCSA Track & TracePDMAPDMA Compliant
System Status: All 14 Zones Nominal · 2026-02-25 05:09 UTC
99.998%
Temperature Compliance Across 2.4M Sq Ft

A climate-controlled fortress where biologics, controlled substances, and cold-chain injectables sit at exactly 2–8°C behind FDA-validated monitoring systems — twenty-four hours without interruption.

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2.4M
Sq Ft
84,000
Pallet Positions
24/7
Monitored
Storage Classes
Ambient · Cold-Chain · Controlled
Monitoring
Continuous Wireless Sensors
Certifications
FDA · DEA · VAWD · cGMP
Scroll to Review Capabilities
01
Independent Climate Zones
14 Zones
Independent Climate Zones
2–8°C
Maintained Continuously
±0.3°C
Temperature Variance
Sensor Array Active

Zone-Level Redundancy, Not Facility-Level

Every one of our 14 climate zones operates on an independent HVAC and refrigeration circuit. A compressor failure in Zone 7 cannot affect Zone 3. Each zone maintains its own dedicated backup refrigeration unit, independent power feed from the UPS bank, and isolated sensor network — so a single-point failure never becomes a facility-wide event.

02
Average Excursion Response Time
< 6 Min
Average Excursion Response Time
90 sec
Backup Refrigeration Spin-Up
847
Alerts Resolved, Zero Losses
Sensor Array Active

Triple-Alert Cascade Before the Product Moves

When a sensor crosses threshold, a triple-alert cascade fires simultaneously: on-site technician pager, facility management platform push notification, and automated backup refrigeration spin-up — all within 90 seconds. Our average documented response time across 847 alert events over 36 months is 5 minutes 42 seconds. No excursion has ever progressed to product impact.

03
Regulatory Audit Pass Rate
100%
Regulatory Audit Pass Rate
7 Yrs
Consecutive Clean Audits
24 Hr
Documentation Turnaround
Sensor Array Active

Seven Consecutive Years. Zero Citations.

FDA 21 CFR Part 211 inspections, DEA Schedule II–V audits, VAWD accreditation reviews, and state board pharmacy inspections. Every one passed without a single critical observation or 483 citation across seven consecutive years. Our compliance team maintains a living audit-ready documentation package — SOP libraries, calibration records, chain-of-custody logs — available to clients on request within 24 hours.

04
Average Client Onboarding
48 Hr
Average Client Onboarding
34
Clients Onboarded, 18 Months
3
First-Commercial Biotechs
Sensor Array Active

From Signed Agreement to First Pallet In

We have onboarded 34 clients in the past 18 months, including three biotech companies shipping their first commercial product. Our standard onboarding package covers storage class qualification, DEA registration verification, chain-of-custody protocol setup, and client portal access — all completed within 48 hours of executed agreement. For controlled substance clients, DEA Schedule II authorization is confirmed before any product transfer.

Operational Record — As of February 2026
2.4MSq Ft
Total Facility Footprint
84,000Positions
Pallet Capacity
99.998%
Temperature Compliance Rate
14Zones
Independent Climate Zones
$0Losses
Product Loss in 7 Years
48 Hr
Average Onboarding Time
VAULT
Schedule Access

The facility passes the audit before you arrive.

Schedule a virtual walkthrough or on-site tour. Select your storage class interest — ambient, cold-chain, or controlled substance — and a Vault operations director will confirm within 4 business hours.

Virtual Walkthrough
60-min guided video tour with Q&A
On-Site Visit
Full facility access with compliance review
// Access Request

Request a Facility Tour

Routed to a dedicated scheduling page. Select tour type, preferred date, and storage class interest.

4-hour confirmation from operations director
Compliance portfolio included with confirmation
DEA and FDA documentation available on request