Steritec Products Mfg. Co., Inc.

Form 483

Englewood, Colorado, United StatesFEI 1000125215Issued February 01, 2017

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1000125215.

Observations3

Issue DateFebruary 01, 2017

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Steritec Products Mfg. Co., Inc.
Location: Englewood, Colorado, United States
FEI Number: 1000125215
Product Type: Devices
Issue Date: February 01, 2017
Country: United States

Inspection History, 2009 to 2026

NAI1

VAI4

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Steritec Products Mfg. Co., Inc. FDA Form 483, Englewood, Colorado, February 1, 2017