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Lonza Houston, Inc — FDA Facility Profile

FEI 3013629214

Lonza Houston, Inc is an FDA-registered facility (FEI 3013629214) located in Houston, TX, US. Registered operations: ANALYSIS; API MANUFACTURE; LABEL; MANUFACTURE; PACK. RegDataLab tracks 1 FDA inspection at this facility.

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What FDA found at this site

Latest inspection
Dec 10, 2020: No Action Indicated (NAI)
Inspections on record
1 (1 NAI)
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
Form 483 and inspection documents
1 in FDA's reading room

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
Dec 10, 2020No Action Indicated (NAI)No citations listed

Form 483s and inspection documents

Facility details

Company
Lonza Houston, Inc
Location
Houston, TX (US)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; API MANUFACTURE; LABEL; MANUFACTURE; PACK
Source
decrs

FDA data resources

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