FDA Inspection 1021136 — BioSpectra, Inc.

BioSpectra, Inc. — FEI 3010476065

The FDA completed an inspection of BioSpectra, Inc. on August 1, 2017 in Bangor, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 1, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bangor, PA (United States)