FDA Inspection 1340178 — Post Oak Innovations, Inc.

Post Oak Innovations, Inc. — FEI 3009770819

The FDA completed an inspection of Post Oak Innovations, Inc. on Oct 8, 2026 in Dallas, 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
Oct 8, 2026
Fiscal Year
2027
Product Type
Devices
Project Area
Compliance: Devices
Location
Dallas, TX (United States)

Citations

IDCFRDescription
23135ISO 13485:2016 Clause 7.3.9Records of design and development changes and their reviews not maintained

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