FDA Inspection 1050458 — Acro Biotech Inc.

Acro Biotech Inc. — FEI 3005670738

The FDA completed an inspection of Acro Biotech Inc. on May 1, 2018 in Rancho Cucamonga, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 1, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Rancho Cucamonga, CA (United States)

Citations

IDCFRDescription
63321 CFR 803.17(a)(3)Lack of System for Timely Submission of Reports