Hypoxic Chamber Replacement Shell

The U.S. Food and Drug Administration’s Office of Acquisition and Grant Services is soliciting a Firm-Fixed Price contract for a Hypoxic Chamber Replacement Shell to replace the cracked outer casing of an existing Coy Lab Products two-person O2 Control Glove Box Hypoxic Chamber, model 8375065. The replacement shell must meet specific technical requirements including a two-person (four-port) glove box configuration with precise control of temperature, pressure, oxygen, carbon dioxide, and humidity, an internal workspace of 59" L x 23" D x 23" H, an integrated airlock for sample transfer, digital controls for airlock and chamber environmental parameters, and an anaerobic kit. The shell must be substantially similar to Coy Lab Products items 8375095 and 8526130. All proposals must be submitted via email to Howard Nesmith by 1:00 PM Central Time on June 17, 2026, referencing solicitation number 75F40126Q134291, and must include comprehensive technical documentation to demonstrate full compliance with all specifications. The solicitation is restricted to small business concerns under a Total Small Business Set-Aside per FAR 19.5, and all offerors must be currently registered and active in SAM.gov with a valid Unique Entity Identifier. The contract requires delivery FOB Destination to the Center for Biologics Evaluation and Research at 10903 New Hampshire Ave, Silver Spring, Maryland 20993, inclusive of all shipping, handling, and delivery charges, with no deliveries permitted on federal holidays. Evaluation will follow a Lowest Price Technically Acceptable (LPTA) process, where the lowest-priced responsive offer that meets all technical requirements will be selected. Acceptance occurs at the destination by the Contracting Officer’s Representative, and payment is contingent upon government acceptance of the item, processed net 30 days post-acceptance through the Treasury’s Invoice Processing Platform. Invoices must comply with FAR 32.905(b), include an invoice log addendum, and for time-and-materials or cost-reimbursement lines, substantiating documentation. The item must conform to Section 508 accessibility standards, requiring an Accessibility Conformance Report based on the Voluntary Product Accessibility Template if any non-compliance exists, with remediation costs borne by the contractor. The Buy American Act and Executive Order