FDA Inspection 1266828 — PRO-TECH Design & Mfg., Inc.

PRO-TECH Design & Mfg., Inc. — FEI 3010531069

The FDA completed an inspection of PRO-TECH Design & Mfg., Inc. on Apr 14, 2025 in Arlington, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 14, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Arlington, TX (United States)

Citations

IDCFRDescription
343221 CFR 820.75(b)(2)Documentation of validated process performance

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.