FDA Inspection 1115908 — Medinatura New Mexico, Inc.

Medinatura New Mexico, Inc. — FEI 1626962

The FDA completed an inspection of Medinatura New Mexico, Inc. on Dec 18, 2019 in Albuquerque, NM. 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 18, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Albuquerque, NM (United States)

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