FDA Inspection 818470 — Trinity Sterile, Inc.

Trinity Sterile, Inc. — FEI 1000123297

The FDA completed an inspection of Trinity Sterile, Inc. on February 13, 2013 in Salisbury, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 13, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Salisbury, MD (United States)

Citations

IDCFRDescription
328621 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate