FDA Inspection 880573 — IndeCon, Inc.

IndeCon, Inc. — FEI 3010056143

The FDA completed an inspection of IndeCon, Inc. on May 29, 2014 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). 3 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 29, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Dallas, TX (United States)

Citations

IDCFRDescription
1241621 CFR 1271.260(e)Storage temperatures recorded, maintained
1243121 CFR 1271.265(e)Procedures and release criteria
1243221 CFR 1271.265(e)Documentation elements for activities

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