FDA Inspection 1071837 — Slater Endoscopy, LLC

Slater Endoscopy, LLC — FEI 3011099779

The FDA completed an inspection of Slater Endoscopy, LLC on Nov 16, 2018 in Miramar, FL. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 16, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Miramar, FL (United States)

Citations

IDCFRDescription
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures

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