FDA Inspection 883470 — Acon Laboratories, Inc.

Acon Laboratories, Inc. — FEI 3003516723

The FDA completed an inspection of Acon Laboratories, Inc. on Jun 11, 2014 in San Diego, CA. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures

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