FDA Inspection 918031 — Breas Medical AB

Breas Medical AB — FEI 3003244771

The FDA completed an inspection of Breas Medical AB on Mar 5, 2015 in Molnlycke. 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
Mar 5, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Molnlycke (Sweden)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
317321 CFR 820.198(d)Evaluation, timeliness, identification