FDA Inspection 973786 — Rockledge Pharmaceutical Manufacturing LLC

Rockledge Pharmaceutical Manufacturing LLC — FEI 1000113139

The FDA completed an inspection of Rockledge Pharmaceutical Manufacturing LLC on May 19, 2016 in Rockledge, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 19, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockledge, FL (United States)

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