FDA Inspection 841056 — Lenstec, Inc.

Lenstec, Inc. — FEI 3001659659

The FDA completed an inspection of Lenstec, Inc. on Jul 18, 2013 in St Petersburg, FL. 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
Jul 18, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
St Petersburg, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
317321 CFR 820.198(d)Evaluation, timeliness, identification