FDA Inspection 1031825 — AMPCARE, LLC

AMPCARE, LLC — FEI 3008273892

The FDA completed an inspection of AMPCARE, LLC on Nov 15, 2017 in Fort Worth, TX. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 15, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Fort Worth, TX (United States)

Citations

IDCFRDescription
232821 CFR 820.22Quality audits - auditor independence
313021 CFR 820.100(a)Lack of or inadequate procedures

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