Labverity
Facility profile

Flamma SpA

Active pharmaceutical ingredient (API) manufacturing · Bulciago · Italy

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed3 registered company locations
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.

Active pharmaceutical ingredient (API) manufacture
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
Voluntary action indicated (VAI)

Dec 15, 2023 · FDA documented observations for voluntary correction.

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 voluntary action indicated inspection.

Doesn’t show

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

Ask next

Ask what was corrected and review any later inspection or follow-up record.

Method and source details
View full inspection and compliance history4 inspection records

FDA inspection history

4 records, Feb 2011 – Dec 2023 · 1 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
Dec 15, 2023VAIDrug Quality Assurance2024
Jul 26, 2019VAIDrug Quality Assurance2019
Mar 13, 2014NAIDrug Quality Assurance2014
Feb 3, 2011VAIDrug Quality Assurance2011

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