FDA Inspection 1061728 — Anesthetic Gas Reclamation Inc.

Anesthetic Gas Reclamation Inc. — FEI 3008492433

The FDA completed an inspection of Anesthetic Gas Reclamation Inc. on August 9, 2018 in Dallas, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 9, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Dallas, TX (United States)

Citations

IDCFRDescription
232821 CFR 820.22Quality audits - auditor independence
342721 CFR 820.50(a)(2)Supplier oversight
405921 CFR 820.22Quality Audits - defined intervals