BioLyte Laboratories, LLC

Form 483

Grand Rapids, Michigan, United StatesFEI 3013171766Issued December 15, 2017

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Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3013171766.

Observations6

Issue DateDecember 15, 2017

Status1 Related Warning Letter

Related Inspections5

Establishment Details

Firm: BioLyte Laboratories, LLC
Location: Grand Rapids, Michigan, United States
FEI Number: 3013171766
Product Type: Drugs
Issue Date: December 15, 2017
Country: United States

Inspection History, 2017 to 2025

NAI1

VAI1

OAI3

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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BioLyte Laboratories, LLC FDA Form 483, Grand Rapids, Michigan, December 15, 2017