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sive and often ambiguous requirements in both  or conduct associated with the qualified [farm or facility] that are mate-
          proposed rules leave plenty of room for alleged  rial to the safety of the food manufactured, processed, packed, or held at
          violations that are in the eye of the beholder,  such [farm or facility].” The agency would then notify the producer of this
          namely the local FDA inspector.           finding, without being required to specify what the alleged problems are,
              Many of WAPF’s comments on the proposed  and the producer would have only ten days to respond.
          rules focused on the ambiguities and potential     Under the proposed rules, the agency can choose whether or not to
          avenues for abuse. In particular, the provisions  provide a hearing before it makes its final determination. And once the
          that govern FDA’s ability to revoke a producer’s  FDA makes a final decision to revoke the exemption, the farmer or facil-
          Tester-Hagan exemption are very problematic.  ity would then have only sixty or one hundred twenty days (depending on
          As proposed by FDA, a local inspector can  which rule) to come into full compliance with the extensive, expensive
          simply allege that revocation “is necessary to  FSMA requirements. In practical terms, almost any small producer tar-
          protect the public health and prevent or mitigate  geted in this way would go out of business. While FDA is unlikely to use
          a foodborne illness outbreak based on conditions  this power often, even a few cases of arbitrary revocations could create a


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