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FDA Inspection 1010928 — STERITECH, INC.

STERITECH, INC. — FEI 2648209

The FDA completed an inspection of STERITECH, INC. on April 26, 2017 in Salinas, PR. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 26, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Salinas, PR (United States)

Facility

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FDA data resources