FDA Inspection 741931 — Exmoor Plastics Limited

Exmoor Plastics Limited — FEI 3002806953

The FDA completed an inspection of Exmoor Plastics Limited on Aug 4, 2011 in Chorley. 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). 7 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 4, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Chorley (United Kingdom)

Citations

IDCFRDescription
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
326321 CFR 820.250(b)Sampling plans
333121 CFR 820.181DMR - not or inadequately maintained
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation
63121 CFR 803.17(a)(1)Lack of System for Event Evaluations

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