FDA Inspection 1118382 — Precision Forms, Inc.

Precision Forms, Inc. — FEI 3010041993

The FDA completed an inspection of Precision Forms, Inc. on Dec 4, 2019 in Butler, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Dec 4, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Butler, NJ (United States)

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