Labverity
Facility profile

PATHEON API, INC.

Testing & analysis · Drug product manufacturing · Florence, SC

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

AnalysisActive pharmaceutical ingredient (API) manufactureManufacture
Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
No action indicated (NAI)

Jun 12, 2026 · No conditions warranted FDA action in this inspection.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

Understand this record

Use the evidence, then ask for fit.

Shows

Registration status and a latest matched no action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

Ask next

Confirm the inspection scope and whether it covered the work you need.

Method and source details
View full inspection and compliance history6 inspection records

FDA inspection history

6 records, Jan 2010 – Jun 2026 · 4 NAI · 2 VAI · 0 OAI

DateClassProject areaCitationsFY
Jun 12, 2026NAIDrug Quality Assurance2026
Jun 28, 2024NAIDrug Quality Assurance2024
Nov 9, 2018VAIDrug Quality Assurance2019
Dec 19, 2014NAIDrug Quality Assurance2015
Jun 8, 2012VAIDrug Quality Assurance2012
Jan 27, 2010NAIDrug Quality Assurance2010

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

Ask about services