FDA Inspection 945199 — Tecomet, Inc.

Tecomet, Inc. — FEI 3003018882

The FDA completed an inspection of Tecomet, Inc. on Aug 19, 2015 in Woburn, MA. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 19, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Woburn, MA (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
328821 CFR 820.90(b)(1)Documentation of disposition, justification, signature

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