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Alive 2 Dive Company Limited FDA Inspection Record

FEI 3016453477 · Inspections, Form 483s, warning letters and import refusals

Alive 2 Dive Company Limited is an FDA-inspected facility (FEI 3016453477) located in Mueang, TH. RegDataLab tracks 1 FDA inspection at this facility.

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What FDA found at this site

Latest inspection
May 3, 2024: Voluntary Action Indicated (VAI)
Inspections on record
1 (1 VAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Import refusals
1

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
May 3, 2024Voluntary Action Indicated (VAI)Procedures not in writing, fully followed (21 CFR 211.22(d))
Absence of Written Procedures (21 CFR 211.100(a))
Review of representative number of batches (21 CFR 211.180(e)(1))
Component identification test (21 CFR 211.84(d)(2))

Facility details

Company
Alive 2 Dive Company Limited
Location
Mueang (TH)
Source
inspections

Import refusals

FDA data resources

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