FDA Inspection 1187279 — Cantor & Barnard Ltd.

Cantor & Barnard Ltd. — FEI 3002807717

The FDA completed an inspection of Cantor & Barnard Ltd. on Nov 3, 2022 in Brackley. 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). 4 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 3, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Brackley (United Kingdom)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
316021 CFR 820.184Lack of or inadequate DHR procedures

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