FDA Inspection 1043176 — New England Life Care, Inc.

New England Life Care, Inc. — FEI 1000159373

The FDA completed an inspection of New England Life Care, Inc. on Mar 2, 2018 in Portland, ME. 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). 5 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 2, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Portland, ME (United States)

Citations

IDCFRDescription
18937FDCA 501(a)(2)(A)Beta-lactam drugs, inadequate sanitation
18944FDCA 501(a)(2)(A)Exposure of personnel in aspectic processing
18963FDCA 501(a)(2)(A)Inadequate HEPA filter, sterile product area
18970FDCA 501(a)(2)(A)Disinfecting and cleaning agents, ISO 5 area
18973FDCA 501(a)(2)(A)Disinfecting materials, aseptic processing area

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