FDA Inspection 1249659 — Cortex Manufacturing Inc.

Cortex Manufacturing Inc. — FEI 3008706707

The FDA completed an inspection of Cortex Manufacturing Inc. on Sep 19, 2024 in Byhalia, MS. 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
Sep 19, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Byhalia, MS (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures