FDA Inspection 1018250 — Coastal Bend Blood Center

Coastal Bend Blood Center — FEI 1671283

The FDA completed an inspection of Coastal Bend Blood Center on Jul 14, 2017 in Corpus Christi, 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: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 14, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Corpus Christi, TX (United States)

Citations

IDCFRDescription
1503021 CFR 606.60(b)Equipment calibration frequency

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