FDA Inspection 877274 — Mediplast Israel Ltd.

Mediplast Israel Ltd. — FEI 3002807555

The FDA completed an inspection of Mediplast Israel Ltd. on Apr 3, 2014 in Yavne. 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). 6 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 3, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Yavne (Israel)

Citations

IDCFRDescription
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
328621 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.